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What is the main use of 1,2-difluoro-4- [[4- (trans-4-propylcyclohexyl) phenyl] ethynyl] benzene?
1% 2C2-diene-4- [4- (trans-4-propylcyclohexyl) phenyl] ethyl] benzene, which is a crucial raw material in the field of organic synthesis. It plays a pivotal role in materials science, especially in the preparation of liquid crystal materials.
Liquid crystal materials, such as liquid crystal displays (LCDs), occupy a central position in modern display technologies. The unique molecular structure of 1% 2C2-diene-4- [4- (trans-4-propylcyclohexyl) phenyl] ethyl] benzene imparts specific physical properties to liquid crystal materials, such as liquid crystal phase stability, suitable phase transition temperature range, and good optical anisotropy. With these properties, liquid crystal molecules can be arranged and oriented in an orderly manner under the action of an electric field, thus achieving precise regulation of the direction and intensity of light propagation, resulting in clear images and text.
In addition, in the field of organic semiconductor materials, 1% 2C2-diene-4- [4- (trans-4-propylcyclohexyl) phenyl] ethyl] benzene may also have applications. Organic semiconductor materials have broad application prospects in flexible electronic devices such as flexible displays, wearable devices, and organic solar cells due to their advantages of light weight, good flexibility, low cost, and solution processing. The special structure of 1% 2C2-diene-4- [4- (trans-4-propylcyclohexyl) phenyl] ethyl] benzene may provide suitable electron transport properties and molecular stacking methods for organic semiconductor materials, improving device performance and stability.
What are the physical properties of 1,2-difluoro-4- [[4- (trans-4-propylcyclohexyl) phenyl] ethynyl] benzene
1% 2C2-diene-4- [[4- (trans-4-methylcyclohexyl) phenyl] ethyl] benzene is an organic compound. This compound has several unique physical properties.
Its melting point is the temperature at which a substance changes from a solid state to a liquid state. The exact value of the melting point of this compound varies depending on the specific purity and measurement conditions. Generally speaking, the melting point of organic compounds is affected by intermolecular forces and structural regularity. In the molecular structure of this compound, the benzene ring interacts with structural units such as cyclohexyl to affect the way the molecule is deposited, which in turn affects the melting point.
The boiling point is the temperature at which a substance changes from a liquid state to a gas state under a specific pressure. In view of the fact that its molecules contain multiple aromatic rings and alkyl structures, there are interactions such as van der Waals forces between molecules, resulting in a relatively high boiling point. During the heating process, sufficient energy needs to be provided to overcome the intermolecular forces before it can boil.
In terms of solubility, according to the principle of similarity dissolution, the compound, as an organic molecule, should have good solubility in organic solvents such as toluene and dichloromethane, because these organic solvents and the compound molecules can form similar intermolecular forces, which is conducive to its dispersion and dissolution. However, the solubility in water is poor, because its molecular polarity is weak, it is difficult to form effective interactions with water molecules.
Density is related to the mass of matter per unit volume. The density of this compound is related to the type, number and spatial arrangement of constituent atoms. Since the molecule contains carbon, hydrogen and other atoms, and has a certain structural complexity, its density should be within the density range of common organic compounds.
The physical properties of this compound are crucial for its application in organic synthesis, materials science and other fields. Melting point and boiling point determine its state change under specific conditions, which affects the choice of reaction conditions; solubility affects its reactivity and processability in different solvent systems; density has certain guiding significance for the design and preparation of related materials.
Are the chemical properties of 1,2-difluoro-4- [[4- (trans-4-propylcyclohexyl) phenyl] ethynyl] benzene stable?
Is the chemical property of 1% 2C2-diene-4- [[4- (trans-4-butylcyclohexyl) phenyl] ethyl] benzene stable? To understand this question, it can be analyzed from its structure. This compound contains a conjugated diene structure, and the conjugated system deloculates electrons and imparts certain stability. However, conjugated dienes have high reactivity. If it is prone to addition reactions, new compounds can be formed in case of electrophilic reagents, and the stability is poor in this regard.
Its molecule also contains a benzene ring structure, which is aromatic. The energy of the system is reduced and the stability is enhanced due to the closure of the conjugated large π bond. The benzene ring electron cloud has high density, although it is prone to electrophilic substitution reaction, the reaction conditions are relatively mild and can maintain a certain stability in general environment.
contains alkyl side chains, and alkyl is the power supply group, which can affect the conjugation system and the distribution of benzene ring electron clouds, and change its chemical activity and stability to a certain extent.
Overall, 1% 2C2-diene-4- [4 - (trans-4-butylcyclohexyl) phenyl] ethyl] benzene has certain stability under specific conditions and environments, but because it contains active structures such as conjugated dienes, its chemical properties are not extremely stable, and it is prone to chemical reactions under certain reaction conditions, resulting in structural changes.
What is the production process of 1,2-difluoro-4- [[4- (trans-4-propylcyclohexyl) phenyl] ethynyl] benzene?
1% 2C2-diene-4- [4- (trans-4-butylcyclohexyl) phenyl] ethyl] benzene is a complex compound in the field of organic synthesis. The preparation process is delicate and complicated, and it will be described in detail.
In the initial stage, suitable raw materials need to be carefully selected. 4- (trans-4-butylcyclohexyl) bromobenzene and 1,2-dibromoethane are both key starting materials. Both are chemically active and play a central role in subsequent reaction steps.
In the first step of the reaction, 4- (trans-4-butylcyclohexyl) bromobenzene and magnesium chips are reacted in an anhydrous ether environment in an inert environment carefully created in a nitrogen atmosphere. The reaction conditions are harsh, and the requirements for anhydrous and anaerobic are extremely high. Magnesium chips are active and react violently in contact with water, so the anhydrous ether solvent needs to be strictly removed from water. During the reaction, magnesium chips react slowly with bromobenzene to form a Grignard reagent. This reagent has extraordinary activity and significant carbon-magnesium bond polarity, laying the foundation for subsequent nucleophilic substitution reactions.
After the Grignard reagent is generated, it is rapidly mixed with 1,2-dibromoethane to initiate a nucleophilic The negatively charged carbon in Grignard's reagent attacks the carbon attached to one of the bromine atoms in 1,2-dibromoethane, and the bromine ions leave to form a carbon-carbon bond. This step constructs the key carbon chain structure, and the product is the intermediate containing butylcyclohexyl phenyl ethyl bromide. The
intermediate is separated and purified to ensure that the purity is up to standard, and then proceeds to the next step. Treat with a strong base such as potassium tert-butanol and put it in a suitable organic solvent such as tetrahydrofuran to initiate a elimination reaction. The strong alkali grabs the hydrogen atom in the intermediate molecule, and the bromine ion leaves to form a carbon-carbon double bond, and obtains 1% 2C2-diene-4- [[4- (trans-4-butylcyclohexyl) phenyl] ethyl] benzene crude product.
The crude product has many impurities and requires a multi-step purification process. First, it is preliminarily separated by column chromatography. Silica gel is used as the fixed phase, and a suitable eluent such as n-hexane and ethyl acetate mixture is eluted. Preliminary separation is achieved according to the polarity difference between each impurity and the product. After recrystallization, a suitable solvent such as ethanol or acetone is selected, and it is slowly crystallized in a suitable temperature range to further improve the purity of the product.
The steps of this synthesis process are closely connected, and the reaction conditions, raw material purity and operation details are extremely demanding. A slight difference in any link may lead to a decrease in the yield or poor purity of the product. Only by strictly controlling the reaction steps can high-quality 1% 2C2-diene-4- [4 - (trans-4-butylcyclohexyl) phenyl] ethyl] benzene products be obtained.
What is the price range of 1,2-difluoro-4- [[4- (trans-4-propylcyclohexyl) phenyl] ethynyl] benzene on the market?
I look at what you said about "1,2-diene-4- [4 - (trans-4-butylcyclohexyl) phenyl] ethyl] benzene", which is an organic compound. However, it is not easy to know its market price range. The price is determined by many factors.
The first to bear the brunt is the purity. If the purity is extremely high and suitable for high-end scientific research or special industrial use, the price will be high; if the purity is slightly lower, it is only for general experiments or basic production, and the price is slightly cheaper.
Furthermore, the scale of production also affects the price. In large-scale production, due to the scale effect, the unit cost may be reduced, and the price will also decrease; if it is produced on a small scale, the cost will be high, and the price will rise.
In addition, the market supply and demand relationship also affects its price. If the demand is strong and the supply is limited, the price will rise; if the market is saturated and the supply is sufficient, the price may be downward.
As far as I know, such compounds occasionally appear in the fine chemical and scientific research reagent markets. If it is ordinary purity, the price per gram may be between tens of yuan and hundreds of yuan; if it is high-purity high-quality products, the price per gram may reach thousands of yuan. However, this is only a rough estimate, and the actual price depends on specific market conditions, merchants and trading conditions.