6-Amino-2,3-difluorophenyl ethanol is one of the organic compounds. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry.
In the way of pharmaceutical research and development, many drug synthesis relies on it as a starting material. Because its structure contains amino groups and phenyl ethanol parts, amino groups are active and reactive, and can react with many reagents such as substitution and condensation; phenyl ethanol structure can endow compounds with specific spatial configuration and physicochemical properties. Based on this, chemists can build complex drug molecular skeletons, and then develop drugs to treat various diseases, such as antibacterial, anti-inflammatory, and anti-tumor drugs.
In the field of materials science, 6-amino-2,3-difluorophenyl ethanol also has potential uses. It can participate in the synthesis of polymer materials, introducing it into the polymer chain through chemical reactions to change the properties of the material. For example, to improve the solubility and thermal stability of the material or to endow the material with special optical and electrical properties, so as to meet the unique needs of different fields for material properties.
In addition, in the basic research of organic synthetic chemistry, this compound provides a good model substrate for studying new reaction mechanisms and exploring reaction conditions due to its unique combination of functional groups. By experimenting with various reactions, chemists can expand the methodology of organic synthesis and provide new ideas and methods for the efficient synthesis of more complex organic molecules.

The synthesis method of 6-amino-2,3-difluorobenzene ethanol is a research in the field of chemical synthesis. To synthesize this substance, there are many common methods.
First, it can be started from a suitable benzene ring derivative. First, take a benzene ring compound with a specific substituent, and then introduce fluorine atoms at a specific position through halogenation reaction to achieve the substitution pattern of 2,3-difluorine. This halogenation reaction requires careful selection of halogenation reagents and reaction conditions to ensure the position selectivity and reaction efficiency of fluorine atom substitution.
Then, through amination reaction, amino groups are introduced into the benzene ring. There are many means of amination, such as using an ammonia source and a suitable catalyst, reacting at a suitable temperature and pressure, so that the benzene ring and ammonia undergo nucleophilic substitution and other reactions to construct an amino group.
Furthermore, the ethanol group is introduced. By means of nucleophilic substitution, the ethanol group-containing reagent reacts with the benzene ring intermediate with fluorine and amino groups, so that the ethanol group is connected to the benzene ring, and the final result is 6-amino-2,3-difluorophenyl ethanol. This step also requires fine regulation of the reaction conditions, such as the reaction solvent, the type and amount of base, etc., to ensure the smooth progress of the reaction and improve the yield and purity of the product.
There is also a synthesis path, which is based on the functional group conversion strategy. Starting from the benzene ring compounds with other convertible functional groups, the functional groups on the benzene ring are sequentially converted to form fluorine atoms, amino groups and ethyl alcohol groups one after another. This process requires careful consideration of the sequence of reactions, reaction conditions and the stability of intermediates, so that each step can achieve the desired effect, and the reactions of each step are compatible with each other, and finally the target product 6-amino-2,3-difluorophenethyl alcohol is synthesized through multi-step reactions. In short, the synthesis of this compound requires following the principle of chemical synthesis, ingeniously designing routes, and carefully controlling reaction conditions to achieve efficient and high-purity synthesis.

6-Amino-2,3-difluorophenyl ethanol, the market price of this substance is difficult to determine. The price in the market often changes due to various reasons, and cannot be held together.
Its market price is determined by the supply of raw materials, the difficulty of production methods, the amount of demand, the distance of business routes, and the smoothness of the current situation. If the raw materials are abundant, the procurement is convenient, and the production is easy and the demand is limited, the price may become cheaper; on the contrary, if the raw materials are rare, the production is complicated, and there are many people seeking, the price will be high.
Looking at the market conditions of the past, the price of similar products also varies. However, today is different from the past, the market conditions are changing rapidly, or the cost is reduced due to the rise of new technologies, or the supply and demand are shifted due to the change of government orders. Therefore, to know the exact price, you need to consult the chemical market, vendors, or check the detailed records of recent transactions and research reports on market conditions. It is difficult to determine the exact price in the market based on speculation alone.

6-Amino-2,3-difluorophenyl ethanol, this is an organic compound. Its physicochemical properties are particularly important and relevant to its application in many fields.
When it comes to physical properties, under normal conditions, 6-amino-2,3-difluorophenyl ethanol is mostly in solid form, but it also varies depending on specific conditions. Its melting point and boiling point are determined by intermolecular forces. The amino and hydroxyl groups in the molecule can form hydrogen bonds, resulting in relatively high melting and boiling points. And because of the fluorine atom, the electronegativity of fluorine is large, which also affects the intermolecular forces.
In terms of solubility, because of its polar groups amino and hydroxyl groups, it should have some solubility in polar solvents such as methanol, ethanol, water, etc. However, due to the non-polar nature of the benzene ring, the solubility in non-polar solvents such as n-hexane is poor.
In terms of chemical properties, amino groups are basic and can react with acids to form salts. In case of hydrochloric acid, corresponding hydrochloric salts can be formed. Hydroxyl groups can participate in esterification reactions and form esters with carboxylic acids under the action of catalysts. Although fluorine atoms on the benzene ring are relatively stable, under certain conditions, such as strong nucleophiles and high temperatures, nucleophilic substitution reactions can also occur.
In addition, the conjugated system of 6-amino-2,3-difluorophenyl ethanol makes it absorb in the ultraviolet light region, which can be analyzed and identified by ultraviolet spectroscopy. Its chemical structure and electronic effect have a great influence on its physical and chemical properties, and have important application value in organic synthesis, medicinal chemistry and other fields.

6-Amino-2,3-difluorophenyl ethanol is also an organic compound. When storing and transporting, many important items must not be ignored.
First words storage. This compound should be placed in a cool, dry and well-ventilated place. Cover its properties or fear heat and moisture. If it is placed in a high temperature and humid place, it may cause deterioration. High temperature can promote its chemical reaction and change its properties; humid gas, or make it absorb moisture, affects its purity. Therefore, when choosing a cool, dry and well-ventilated place to ensure its stability.
Furthermore, when storing, it must be isolated from oxidants, acids, bases and other substances. Due to its chemical properties, or violent reactions with such substances, it is dangerous. Such as oxidizing agents, or oxidation reactions with 6-amino-2,3-difluorophenyl ethanol, or heat generation, fire, or even explosion; contact with acids and bases may also cause chemical reactions, damage their quality, and may be dangerous.
As for transportation, there are also many precautions. Packaging must be tight and firm. Strong packaging can prevent collision and vibration during transportation and cause leakage. Leakage not only causes compound loss, but also poses a hazard to the environment and personnel.
During transportation, temperature should also be controlled to avoid high temperature. High temperature environments may cause compounds to evaporate and decompose, generating harmful gases, endangering the safety of transportation personnel and polluting the environment. And the transportation vehicle should be clean and free of other chemicals, so as not to interact with it and cause danger.
In summary, 6-amino-2,3-difluorobenzene ethanol should be stored and transported with caution in the environment, isolation, packaging, and temperature control to prevent problems before they occur and ensure its safety and quality.