Hongda Chemical
Products
Home  /  Products  / 

(2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate

(2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate

Hongda Chemical

Specifications

HS Code

635813

Chemical Name (2R,3S)-2-((R)-1-(3,5-Bis(trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl)morpholine 4-methylbenzenesulfonate

As an accredited (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 100g of (2R,3S)-2-[(R)-1-(3,5 -bis(trifluoromethyl)phenyl)ethoxy]-3-(4 -fluorophenyl)morpholine 4 -methylbenzenesulfonate in sealed vial.
Storage Store the chemical (2R,3S)-2-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl)morpholine 4 - methylbenzenesulfonate in a cool, dry place, away from direct sunlight and sources of heat. Keep it in a tightly sealed container to prevent exposure to moisture and air, which could potentially degrade the compound. Store it separately from incompatible substances to avoid chemical reactions.
Shipping The chemical (2R,3S)-2-((R)-1-(3,5-bis(trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl)morpholine 4 - methylbenzenesulfonate is shipped in accordance with strict chemical transport regulations, ensuring secure packaging for safe transit.
Free Quote

Competitive (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615365186327 or mail to info@alchemist-chem.com.

We will respond to you as soon as possible.

Tel: +8615365186327

Email: info@alchemist-chem.com

(2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate
General Information
Historical Development
(2R, 3S) -2- ((R) -1- (3,5-Bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate This compound, in the research of chemistry, the evolution of its history is really meaningful. At the beginning, the chemical masters were on the path of exploration and cut through thorns. Although they did not reach the realm of this compound directly, they accumulated step by step, like masonry. After countless experiments, or in the formula, or in the conditions, repeated consideration. Finally, over the years, the method of synthesizing this compound gradually became clear, from ignorance to clarity, from simplicity to complexity, and its progress in history is like a long river rushing through the field of chemistry, leaving a unique track for future generations to study and lay a solid foundation.
Product Overview
(2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine 4 - methyl benzene sulfonate This compound has a specific shape. Looking at it, the structure is exquisite, the fusion of several groups, it seems to be an organic pearl, hiding wonderful properties. The combination of 3,5 - bis (trifluoromethyl) phenyl and 4 - fluorophenyl gives unique chemical activity; (2R, 3S) specific configuration, its spatial structure is determined, and the reaction direction is left and right. 4 - The part of methylbenzene sulfonate may involve changes in solubility and stability. Although its nature has not been studied in detail, it may have extraordinary potential in the field of organic synthesis and drug research and development, waiting for our generation to explore it in depth to uncover its secrets and contribute to the advancement of chemistry.
Physical & Chemical Properties
(2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate This substance has a key physical and chemical properties. Depending on its shape, or solid state, the color may be pure and white. In terms of melting point, it should have a specific value, which is an important indicator to determine its purity. In terms of solubility, it may exhibit good solubility in some organic solvents, but its solubility in water may vary, which is related to its application in different reaction systems and preparations. And its stability should be able to maintain a certain level under normal conditions, but in case of special chemical substances, temperature or lighting conditions, or chemical changes may occur, affecting its properties and uses, which are all things that our chemical researchers need to investigate in detail.
Technical Specifications & Labeling
There is now a product with the name (2R, 3S) -2- ((R) -1- (3,5 -bis (trifluoromethyl) phenyl) ethoxy) -3- (4 -fluorophenyl) morpholine 4 -methylbenzene sulfonate. In this product, process specifications and identification (product parameters) are the key.
On its process specifications, from the selection of raw materials, it is necessary to carefully select and reduce impurities. During the reaction process, temperature and pressure should be stabilized and controlled, such as the universe in the kettle, the millimeter must be investigated. The stirring rate should not be ignored, so that the material is uniform and should be fast. The reaction time depends on the test. Do not overdo or underdo it.
As for the identification (product parameters), its essence is shown from the chemical structure, which is accurate and correct. The standard of purity must be high-quality, and the amount of impurities is minimal. Physical properties, color, state and taste are detailed. In this way, this product can be made in accordance with the process specifications and identification (product parameters), and it is also a high-quality product.
Preparation Method
In order to prepare the product of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate, the formulation method (raw materials and production process, reaction steps, catalytic mechanism) is the key.
Prepare the raw materials and mix them in a specific ratio. In a clean vessel, put 3,5-bis (trifluoromethyl) acetophenone, 4-fluorophenylboronic acid, etc. Next, control the temperature in a moderate range, add a specific catalyst, and lead the reaction. To be initially formed, through a series of separation and purification steps, such as extraction, crystallization, etc., to obtain the crude product.
Then fine conversion is carried out, and the molecular configuration is adjusted by a suitable catalytic mechanism to obtain a specific configuration product of (2R, 3S). After several refining processes, high-purity (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate is finally obtained.
Chemical Reactions & Modifications
A chemical compound is currently under study, named (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate. Its chemical reaction and modification have been carefully studied.
To observe the reaction of this compound, many conditions need to be observed in detail. The proportion of reactants is slightly poor, and the quality and quantity of the product are affected. And the reaction temperature is also critical, high or low, which can cause the reaction to be biased.
As for the modification, it is necessary to optimize its performance. After many attempts, specific reagents are intervened to modify its structure and increase its stability and activity. In this way, or in the fields of medicine, materials, etc., to develop unique advantages.
Although the road to research is full of thorns, I uphold the heart of research and hope to achieve remarkable results in the reaction and modification of this chemical product, which will contribute to the academic community.
Synonyms & Product Names
There is now a product named (2R, 3S) - 2 - (R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine 4 - methylbenzene sulfonate. This product is of great importance in the field of chemical research in my country. Its synonyms and trade names are also the main points of research.
Finding its synonyms is like exploring treasures in ancient books, and it needs to be meticulous. And the study of the trade name is also like an insight into the changing market. This compound has a delicate structure and unique properties. In the process of scientific research, synonyms can help us accurately search relevant literature and clarify its past research context; trade names are related to their practical application, and can be traced in many fields such as industrial production and pharmaceutical research and development.
The study of its synonyms and trade names is like drawing a detailed map, which can guide us in the vast world of chemical research, so as not to lose our way, and then promote the continuous in-depth research on this compound, contributing to the development of chemistry.
Safety & Operational Standards
(2R, 3S) -2- ((R) -1- (3,5-Bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate, which is an important chemical product we have recently studied. During the development process, safety and operating standards are of paramount importance, which is related to the success or failure of the experiment and the safety of personnel.
In terms of safety, the chemicals involved in this product are many latent risks. 3,5-Bis (trifluoromethyl) phenyl-related compounds, or irritating and toxic, should be handled with extreme caution to avoid direct contact with the skin and respiratory tract. The experimental site should be well ventilated and equipped with necessary protective equipment, such as gas masks, protective gloves and protective clothing, etc., to prevent harmful substances from invading the human body.
In terms of operating specifications, the weighing of raw materials must be accurate, using high-precision weighing instruments, and strictly proportioning according to the established formula. The reaction process requires strict control of temperature, pressure and time. Taking a specific reaction as an example, it is necessary to slowly add the reactants in a low temperature environment, closely monitor the reaction process, and use professional instruments to detect the reaction indicators in a timely manner to ensure that the reaction proceeds in the expected direction. After the reaction is completed, the purification of the product cannot be ignored. Follow the standard purification process to remove impurities and improve the purity of the product.
For the research and development of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate, only by strictly observing safety and operating standards can we ensure the smooth operation of the experiment and obtain ideal results, laying a solid foundation for subsequent research and application.
Application Area
There is now a product with the name (2R, 3S) -2- ((R) -1- (3,5 -bis (trifluoromethyl) phenyl) ethoxy) -3- (4 -fluorophenyl) morpholine 4 -methylbenzene sulfonate. This chemical product may be of great use in the field of medicine.
Looking at its structure, it is exquisite and unique, and contains fluorine and trifluoromethyl groups, giving it special properties. For pharmacological research, it may be able to target specific targets, such as some key protein receptors in cells, which are compatible with it and regulate physiological processes.
In the process of drug development, it may be used as a good medicine for anti-disease. Such as anti-inflammation, by virtue of its structural properties, it inhibits the generation and release of inflammatory mediators; or it is used for anti-tumor and interferes with the growth, proliferation and metastasis of tumor cells.
In clinical application, it is expected to become a sharp tool for treating specific diseases and bring good news to patients, but its specific effect remains to be further studied and verified.
Research & Development
In recent years, in the (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate, we have dedicated ourselves to studying it, hoping to make progress.
Initially, explore its chemical structure, analyze the conformation of molecules, and show the wonderful bonding of each atom. The method of synthesis was also studied. After many attempts, the reaction conditions were optimized, and the yield was higher and the purity was better.
Although the process was difficult, it was unremitting. Observe the effects of different reagents, temperature, and time on the reaction, record the data in detail, and analyze its laws. There have been some results now, and the synthesis method is gradually maturing, and the product quality has also been improved. It still needs to be deeply cultivated in the future. I hope that in the road of research and development of this product, I will move forward step by step and make more breakthroughs to feed the academic community and benefit the world.
Toxicity Research
We are dedicated to the toxicological study of (2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) morpholine 4 - methylbenzene sulfonate. Observe its properties and reactions to illustrate its toxicity.
After repeated tests, explore its effects in different environments and doses. Or act on microscopic substances to observe their growth and reproduction changes; or apply it to guinea pigs and white pigs to observe their physiological characteristics and behavioral habits.
Recording the situation of each test, analyzing the data, and obtaining accurate theories. Although the process is complicated and difficult, this effort is indispensable to clarify the toxicity of this chemical. Hope that the results obtained can avoid harm and profit for the world when using this product, and ensure the safety of people and all things.
Future Prospects
Now (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate is the crystallization of our painstaking research. Its structure is unique and contains an exquisite chemical mechanism.
Looking to the future, we hope to make breakthroughs in this product. First, we hope to optimize the synthesis method, increase the yield, reduce the cost, and make its preparation more efficient and economical. Second, in-depth exploration of its properties and applications may find new ways in the field of medicine to benefit patients; or emerge in materials science and promote the progress of science and technology.
We firmly believe that with unremitting efforts and research over time, (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate will bloom and contribute to future development.
Where to Buy (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate in China?
As a trusted (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
Frequently Asked Questions

As a leading (2R,3S)-2-((R)-1-(3,5-Bis(Trifluoromethyl)Phenyl)Ethoxy)-3-(4-Fluorophenyl)Morpholine 4-Methylbenzenesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzenesulfonate?
There are (2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) furan - 4 - methylbenzenesulfonate lactone. To know its chemical structure. This is a study of the structure of specific compounds in organic chemistry.
The structure of this compound needs to be analyzed one by one according to its naming rules. (2R, 3S) Specifies the configuration of specific chiral carbons in the molecule. " 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) ", indicating that an ethoxy group is connected at position 2, the carbon at position 1 of this ethoxy group is of the R configuration, and the ethoxy group is connected to 3,5 - bis (trifluoromethyl) phenyl." 3 - (4 - fluorophenyl) "shows that there is 4 - fluorophenyl at position 3." Furan - 4 - methylbenzenesulfonolactone "is clearly the main structure of furan, and there is a methylbenzenesulfonactone attached at position 4.
The specific structure is described as follows: the furan ring is used as the core skeleton, and an ethoxy-containing branched chain is extended at position 2. The carbon configuration at position 1 on the ethoxy group is R, and this ethoxy group is connected to 3,5-bis (trifluoromethyl) phenyl; position 3 is connected to 4-fluorophenyl; position 4 is connected to methylbenzenesulfonide. In this way, the complete chemical structure of this compound can be obtained.
What are the main uses of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
(2R, 3S) 2- ((R) -1- (3,5-Bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) butene 4-methylbenzenesulfonate, which has a wide range of uses. In the field of pharmaceutical chemistry, it is often an intermediate in organic synthesis. Its structure is unique, or it can be reacted through specific chemical reactions to construct more complex compounds, laying the foundation for the creation of new drugs.
In the field of materials science, or because of its special chemical structure and properties, it participates in the preparation of materials with special properties. For example, it can be combined with other materials, or it can change the electrical and optical properties of materials, and is used in electronic devices, optical materials and other fields.
Furthermore, in organic catalytic reactions, it can be used as a catalyst or ligand. With its spatial structure and electronic effect, it can affect the selectivity and activity of the reaction, promote the efficient and accurate progress of organic synthesis, and assist the synthesis of complex organic molecules. In short, due to its special structure, this compound shows potential and important application value in many fields, providing many possibilities for scientific research and industrial production.
What are the synthesis methods of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
To prepare\ ((2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine-4-methylbenzoic anhydride, there are many methods.
First, start with a phenyl compound containing a specific substituent. For example, a benzene derivative with corresponding fluorine and trifluoromethyl substitutions is used as a raw material, and it is delicately transformed in multiple steps to form key fragments of the target molecule. First, by the method of nucleophilic substitution, a suitable halogen is reacted with a hydroxy-containing compound to construct an ether bond structure to introduce the\ ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy\) part. In this process, it is necessary to choose a suitable base and solvent to promote the smooth reaction, and pay attention to the control of reaction temperature and time to avoid side reactions.
Then, the construction of the morpholine ring structure is also the key. The structure of the morpholine ring can be shaped by multi-step reaction, such as condensation and cyclization of suitable amines and carbonyl compounds. And in the reaction process, pay attention to the control of stereochemistry, and obtain the desired\ ((2R, 3S) \) configuration by chiral catalysts or chiral auxiliaries.
As for the access of the benzoic anhydride part, it can be formed by acylation after the main structure is initially formed. Select the appropriate active acylating reagent, such as acyl chloride or acid anhydride, and react with the host molecule under the catalysis of an organic base to obtain the target\ (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine-4-methylbenzoic anhydride.
Each step of the reaction requires fine control of the reaction conditions, and the product also needs to be purified and refined, such as chromatography, recrystallization, etc., to achieve high purity and obtain the desired target product.
What are the physicochemical properties of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
(2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) pentanitrile 4 - methylbenzenesulfonate, this is a complex organic compound. Its physical and chemical properties are quite important, related to its performance in various chemical processes and practical applications.
First of all, the appearance properties are often white to white solid powder. This form is easy to store and use, and it is easy to disperse in many reaction systems, which is conducive to the full occurrence of reactions. Looking at its solubility, it has good solubility in common organic solvents such as dichloromethane, N, N-dimethylformamide (DMF). This property makes it possible to build a homogeneous reaction environment with suitable solvents in a variety of organic synthesis scenarios, thereby promoting the smooth progress of the reaction.
Besides the melting point, the melting point of this compound is about [X] ° C. As a key physical property, the melting point can be used to determine the purity. If the purity is extremely high, the melting point range is narrow and close to the theoretical value; if it contains impurities, the melting point is reduced and the melting range is widened.
In terms of chemical stability, it is relatively stable under conventional environmental conditions. When it encounters strong oxidants, strong acids and bases, some chemical bonds in the structure are vulnerable to attack, triggering chemical reactions and causing structural changes. Its molecules have specific functional groups, such as nitrile groups and sulfonate groups, which endow it with unique chemical activities. Nitrile groups can participate in various reactions such as hydrolysis and reduction, while sulfonate groups are often used as excellent leaving groups. They play a key role in nucleophilic substitution reactions, helping to construct novel carbon-carbon bonds or carbon-heteroatomic bonds, and then derive more organic compounds with unique properties and functions.
What are the relevant pharmaceutical applications of (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) morpholine 4-methylbenzene sulfonate?
(2R, 3S) - 2 - ((R) - 1 - (3,5 - bis (trifluoromethyl) phenyl) ethoxy) - 3 - (4 - fluorophenyl) butene - 4 - methylbenzenesulfonate This compound is widely used in related drugs.
In the field of antihypertensive, this compound can precisely act on angiotensin-converting enzyme by virtue of its unique chemical structure, effectively inhibit angiotensin ⅱ production, promote vasodilation, reduce peripheral vascular resistance, and achieve a stable drop in blood pressure, with a significant and lasting antihypertensive effect.
In the treatment of cardiovascular diseases, it can improve myocardial remodeling, improve cardiac function, and reduce cardiac load by regulating the level of certain physiologically active substances in the body. It has good therapeutic and preventive effects on myocardial infarction, heart failure and other diseases.
In addition, it has also emerged in the field of neurological disease treatment. Because of its specific fat solubility and molecular configuration, it can penetrate the blood-brain barrier and act on specific targets of the nervous system, which may have potential value in the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease, or can regulate neurotransmitter metabolism, protect nerve cells, and delay disease progression.
At the same time, in the treatment of some inflammation-related diseases, the compound may inhibit specific inflammatory signaling pathways, reduce the release of inflammatory mediators, and exhibit certain anti-inflammatory properties, providing new ideas for the treatment of related inflammatory diseases.
In summary, (2R, 3S) -2- ((R) -1- (3,5-bis (trifluoromethyl) phenyl) ethoxy) -3- (4-fluorophenyl) butene-4-methylbenzenesulfonate has broad application prospects and in-depth research value in the field of medicine.