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1-Chloro-3-(Trifluoromethyl)-5-(3,3,3-Trifluoroprop-1-En-2-Yl)Benzene

Linshang Chemical

Specifications

HS Code

569544

Chemical Formula C11H5ClF6
Molecular Weight 298.6

As an accredited 1-Chloro-3-(Trifluoromethyl)-5-(3,3,3-Trifluoroprop-1-En-2-Yl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 100 - gram vial packaging for 1 - chloro - 3 - (trifluoromethyl) - 5 - (3,3,3 - trifluoroprop - 1 - en - 2 - yl)benzene.
Storage 1 - Chloro - 3 - (trifluoromethyl) - 5 - (3,3,3 - trifluoroprop - 1 - en - 2 - yl)benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container to prevent leakage and exposure to air or moisture. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions.
Shipping 1 - chloro - 3 - (trifluoromethyl) - 5 - (3,3,3 - trifluoroprop - 1 - en - 2 - yl)benzene is shipped in specialized, well - sealed containers. These containers are designed to prevent leakage and ensure safe transport in compliance with chemical shipping regulations.
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1-Chloro-3-(Trifluoromethyl)-5-(3,3,3-Trifluoroprop-1-En-2-Yl)Benzene 1-Chloro-3-(Trifluoromethyl)-5-(3,3,3-Trifluoroprop-1-En-2-Yl)Benzene
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Frequently Asked Questions

As a leading 1-Chloro-3-(Trifluoromethyl)-5-(3,3,3-Trifluoroprop-1-En-2-Yl)Benzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of 1-chloro-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-ene-2-yl) benzene?
1 + -Deuterium-3- (triethylmethyl) -5- (3,3,3-triethylpropylene-1-alkyne-2-yl) benzene, which is in the scope of "Tiangong Kaiwu", is often involved in the firing of dansa and various gold stones.
The technique of burning Fudan sand has been around since ancient times. In order to obtain pure mercury, it is often based on Dansha, supplemented by various medicinal stones, during which this 1 + -deuterium-3- (triethyl) -5- (3,3,3-triethylpropylene-1-alkynyl-2-yl) benzene is used as a medium to help its reaction, so that the precipitation of mercury in Dansha is more smooth. Because of its special properties, it can interact with Dansha and various medicinal stones to promote their chemical changes, thereby improving the purity and yield of mercury.
Furthermore, in the industry of gold and stone refining and casting, if you want to make the utensils more firm and better in color, you may also use it. When casting a sword, the material of the sword body needs to be tempered and mixed in many ways. Incorporating this benzene into the material of the casting sword in an appropriate proportion can change its metallographic structure, making the blade sharper and tougher, and the sword body has a different luster. This is because it can be fused and reacted with metal elements at high temperature to adjust the characteristics of the metal, thus forming a good tool.
It is also useful in the art of paint modulation. Ancient painters wanted to obtain fresh and lasting colors, and they often used natural minerals and plants as sources to make paints through complicated processes. 1 + -deuterium-3- (triethylmethyl) -5- (3,3,3-triethylpropylene-1-alkyne-2-yl) benzene can be used as a blending aid to make the particles of the pigment more delicate and uniform, and enhance the adhesion and weather resistance of the pigment, so that the painting lasts for a long time and the color is still bright.
What are the physical properties of 1-chloro-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-ene-2-yl) benzene
1 + -Alkane-3- (triethylmethyl) -5- (3,3,3-triethylpropylene-1-alkyne-2-yl) benzene has the following physical properties:
Its color state is mostly liquid at room temperature, and it is clear and transparent in appearance. It is like the quality of glaze. It has a sparkling luster under light, and it also has a solid state, depending on its molecular structure and external conditions.
In terms of its smell, it has a special aromatic smell, which is different from the common smell. Although this smell is not strong and pungent, it has a unique recognition and can be retained in the air for a while.
As for the boiling point, due to the presence of different groups such as alkynyl and alkyl in the molecule, under the interaction, the boiling point is higher, and it needs to reach a certain temperature before it can be converted from liquid to gaseous state. This characteristic makes it capable of maintaining a liquid state in a higher temperature environment.
In terms of melting point, due to the orderly arrangement of different atoms and groups in the molecular structure, the melting point also has its specific value under the influence of mutual forces. At this temperature, the solid state and the liquid state can be in equilibrium.
In terms of solubility, in organic solvents, such as ethanol, ether, etc., it can be well miscible. This is because of the principle of similar compatibility, and the force between the molecules and the organic solvent molecules is suitable. However, in water, the solubility is not good. Because of its weak molecular polarity, it is difficult to form an effective effect with water molecules, so it mostly floats on the water surface and does not mix.
The density is slightly less than that of water. When it is poured into water, it can be seen that it floats on the surface of the water body, and the boundary with water is clear. This is because the molecular mass distribution is different from that of water molecules.
The physical properties of this substance are determined by its unique molecular structure. The interaction of different atoms and groups in the molecule makes it exhibit such physical properties. In many fields such as chemical industry and medicine, this physical property has a profound impact on its application.
What are the chemical properties of 1-chloro-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-ene-2-yl) benzene
This is 1-bromo-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-alkyne-2-yl) benzene, which is quite rich in chemical properties.
From the perspective of reactivity, the bromine atom in this compound has nucleophilic substitution reactivity. Because of its carbon-bromine bond, bromine is more electronegative, which makes the carbon partially positively charged and vulnerable to attack by nucleophilic reagents. For example, under appropriate alkali and solvent conditions, substitution reactions can occur with nucleophiles such as alkoxides and amines, and bromine atoms are replaced by corresponding nucleophilic groups to generate new organic compounds, whereby functional group conversion and modification on the benzene ring can be realized, which is used to construct more complex organic molecular structures.
Furthermore, the alkynyl group part of the molecule is rich in electrons and has high reactivity. The alkynyl group can undergo a variety of reactions, such as electrophilic addition reactions with electrophilic reagents. Taking hydrogen halide as an example, the alkynyl group can be added to it to form halogenated olefin derivatives. In this reaction, the alkynyl π electron cloud is easily attracted by the electrophilic reagent, forming a carbon positive ion intermediate, and then the halogen ion attacks to form an addition product. And the alkynyl group can also participate in metal catalytic coupling reactions, such as Sonogashira reaction. Under the action of palladium and other metal catalysts, it is coupled with aryl halides or vinyl halides to form carbon-carbon bonds, which greatly expands the application of this compound in organic synthesis and helps to synthesize various organic materials and pharmaceutical intermediates with special structures and functions.
In addition, the presence of trifluoromethyl gives the compound unique properties. Trifluoromethyl has strong electron absorption, which can affect the electron cloud density distribution of benzene ring, which in turn affects the reactivity of other groups on the benzene ring. At the same time, trifluoromethyl compounds often have good fat solubility and chemical stability. In the field of drug development, such structures can often improve the bioavailability, metabolic stability and other pharmacokinetic properties of drug molecules.
As a stable conjugate system, the benzene ring itself is relatively stable, but under specific conditions, such as the action of strong oxidants, or high temperatures and catalysts, oxidation and substitution reactions can also occur. In summary, the rich chemical properties of this compound make it show broad application prospects in organic synthesis, pharmaceutical chemistry and other fields.
What are the synthesis methods of 1-chloro-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-ene-2-yl) benzene
To prepare 1-bromo-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-alkyne-2-yl) benzene, the synthesis methods are roughly as follows:
First, benzene is used as the starting material. First, benzene and bromine are substituted, and bromine atoms are introduced into the benzene ring to generate bromobenzene. This reaction requires a slow reaction of bromine and benzene under the catalysis of iron or iron salts to obtain bromobenzene. Then, through a suitable nucleophilic substitution reaction, trifluoromethyl is introduced into the benzene ring. A reagent containing trifluoromethyl can be used to react with bromobenzene under specific conditions to obtain 1-bromo-3- (trifluoromethyl) benzene. Next, 1-bromo-3- (trifluoromethyl) benzene is reacted with a reagent containing 3,3,3-trifluoropropyl-1-alkynyl-2-yl. This reaction requires fine regulation of reaction conditions, such as temperature, solvent, catalyst, etc., and finally results in the target product 1-bromo-3- (trifluoromethyl) -5- (3,3,3-trifluoropropyl-1-alkyne-2-yl) benzene.
Second, another approach can also be found. Start from compounds with some target structures. For example, benzene derivatives containing 3,3,3-trifluoropropyl-1-alkyne-2-yl are synthesized first, and then other positions on the benzene ring are modified. First, a benzene ring structure containing 3,3,3-trifluoropropane-1-alkyne-2-group is constructed, which can be achieved by the related reaction of alkynes and benzene derivatives. Then, the intermediate is brominated, and bromine atoms are selectively introduced at suitable positions, while ensuring that trifluoromethyl and 3,3,3-trifluoropropane-1-alkyne-2-group are not affected. This requires precise control of the reaction conditions, the use of suitable bromination reagents and reaction aids, and the synthesis of the target product.
Third, the strategy of gradually building carbon-carbon bonds can also be considered. Small molecular fragments containing bromine, trifluoromethyl and 3,3,3-trifluoropropyl-1-alkynyl-2-groups were synthesized respectively, and then these fragments were connected one by one by means of methods such as palladium-catalyzed coupling reactions. First, bromine-containing aryl halides, trifluoromethyl-containing nucleophiles, and alkyne derivatives containing 3,3,3-trifluoropropyl-1-alkynyl-2-groups were prepared. Then, under the action of palladium catalysts and ligands, the coupling reactions were carried out in a suitable order. This process requires careful consideration of factors such as reaction sequence, catalyst dosage, reaction time, etc., in order to achieve efficient and selective synthesis of the target compound 1-bromo-3- (trifluoromethyl) -5- (3,3,3-trifluoropropyl-1-alkyne-2-yl) benzene.
Precautions for storing and transporting 1-chloro-3- (trifluoromethyl) -5- (3,3,3-trifluoropropylene-1-ene-2-yl) benzene
When storing and transporting benzene with 1 + -neon-3- (triethylmethyl) -5- (3,3,3-triethylpropylene-1-alkyne-2-yl) benzene, there are several things to pay attention to.
First of all, these substances are mostly chemically active, or active. Although neon is an inert gas, it is co-located with other substances or reacts due to environmental changes. And benzene derivatives containing triethylmethyl, triethylpropynyl and other groups have complex chemical properties. When storing, it must be stored in a dry, cool and well-ventilated place, protected from direct sunlight, to prevent its decomposition or chemical reaction due to temperature and light.
Second, during transportation, make sure that the packaging is tight and leak-free. Because it may be volatile, if the packaging is damaged, it will escape from the outside, or cause environmental pollution, and it is also harmful to the health of the transporter. Furthermore, such substances may be flammable, such as alkynyl-based structures, which can easily cause combustion or even explosion in case of open flames and hot topics. Therefore, when transporting, keep away from fire and heat sources, and the means of transportation should be equipped with fire extinguishing and emergency treatment equipment.
In addition, the storage and transportation place should be managed by a special person, and the warehousing and transportation conditions should be noted in detail. Operators should be professionally trained and familiar with their characteristics and emergency response methods. In case of leakage, take effective measures as soon as possible, such as evacuating the crowd, blocking the fire source, and adsorbing and cleaning with suitable materials. In short, in the storage and transportation of 1 + -neon-3- (triethyl methyl) -5- (3,3,3 -triethylpropylene-1-ethylene-2-yl) benzene, proceed with caution and strictly abide by regulations to ensure safety.