2e 4 4 4 Trifluorobut 2 En 1 Ol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(2E)-4,4,4-trifluorobut-2-en-1-ol
Name (2E)-4,4,4-trifluorobut-2-en-1-ol
Molecular Formula C4H5F3O
Molecular Weight 126.08
Chemical Formula C4H5F3O
Molar Mass 126.08 g/mol
Appearance Colorless liquid (estimated)
Boiling Point Data needed
Melting Point Data needed
Density Data needed
Solubility In Water Data needed
Vapor Pressure Data needed
Flash Point Data needed
Refractive Index Data needed
Chemical Formula C4H5F3O
Molar Mass 126.08 g/mol
Appearance colorless liquid
Boiling Point 110 - 112 °C
Melting Point N/A
Density 1.27 g/cm³
Solubility In Water slightly soluble
Vapor Pressure N/A
Flash Point 30 °C
Refractive Index 1.355
Chemical Formula C4H5F3O
Molecular Weight 128.076 g/mol
Appearance colorless to light yellow liquid
Boiling Point 104 - 106 °C
Density 1.248 g/mL at 25 °C
Flash Point 28 °C
Solubility In Water slightly soluble
Vapor Pressure 3.7 hPa at 20 °C
Refractive Index 1.3785 - 1.3805
Pka 12.9
FAQ

What is the main use of (2E) -4,4,4-trifluorobutyl-2-ene-1-ol?

What are the main uses of (diethyl) -4,4,4-trifluorobutyl-2-ethylene-1-ol? The following answer is in the classical Chinese format of "Tiangong Kaiwu":

(diethyl) -4,4,4-trifluorobutyl-2-ethylene-1-ol, which is widely used in the chemical industry of this world. First, it is a key raw material in the process of organic synthesis. Due to its unique structure, special functional groups can be introduced through various reactions, such as nucleophilic addition and substitution, to prepare other organic compounds, which is essential for the creation of new drugs and fine chemicals.

Furthermore, in the field of materials science, it is also useful. It can be used as a monomer, polymerized to form a polymer material with special properties, or blended with other substances to improve the properties of the material, such as improving the heat resistance and chemical corrosion resistance of the material, making it suitable for harsher environments.

In addition, in some specific catalytic reactions, (diethyl) -4,4,4-trifluorobutyl-2-alkyne-1-ol can be used as an auxiliary agent, which affects the rate and selectivity of the catalytic reaction, and helps the catalyst to better exert its efficiency, optimize the process of the reaction, and improve the quality and yield of the product.

In conclusion, (diethyl) -4,4,4-trifluorobutyl-2-alkyne-1-ol is a compound, but it plays an important role in many fields such as chemical industry, materials, catalysis, etc., and promotes the development and progress of various technologies.

What are the physical properties of (2E) -4,4,4-trifluorobutyl-2-ene-1-ol

(2E) -4,4,4-trifluorobutyl-2-ene-1-ol-1-aldehyde, this physical property is complex and delicate, let me tell you in detail.

It is volatile and can slowly escape in the air at room temperature, like light smoke. This volatilization makes it possible to smell a special smell around, but this smell is not pungent and intolerable, but has a unique rhyme, or it can be explored.

Looking at its solubility, it can be well integrated in organic solvents, such as ethanol and ether, just like fish entering water, which is intimate. However, in water, its solubility is limited, only slightly soluble in water, and seems to remain slightly alienated from water.

When it comes to stability, under normal environmental conditions, it can still maintain the stability of its own structure, just like a monarch sitting in a castle, as stable as Mount Tai. In case of strong acid, strong alkali, or extreme conditions of high temperature, its structure is vulnerable to impact and change, just like a castle is under attack from foreign enemies and is shaky.

Furthermore, its boiling point has a fixed number. When it reaches a certain temperature limit, it will change from liquid to gaseous state to achieve morphological change. The melting point is also one of the characteristics. At a specific low temperature, it solidifies from a flowing state to a solid state. If it solidifies over time, it shows a different style.

Its density is also the key to physical properties. Compared with common liquids, there may be differences, which can be used to distinguish it from other things. This kind of physical property is the unique label of (2E) -4,4,4-trifluorobutyl-2-ene-1-ol-1-aldehyde, which opens a window of exploration for researchers in the field of chemistry and helps them clarify the mysteries and uses of this substance.

What are the chemical properties of (2E) -4,4,4-trifluorobutyl-2-ene-1-ol

(2E) -4,4,4-trifluorobutyl-2-alkyne-1-ol is an organic compound with unique chemical properties.

This substance contains alkynyl and alcohol hydroxyl groups, with high alkynyl unsaturation and active reactivity. Addition reactions can occur, such as addition with hydrogen, and with appropriate catalysts, it can be gradually hydrogenated to form olefins or alkanes; addition with hydrogen halides, following the Markov rule, hydrogen atoms are added to unsaturated carbon atoms containing more hydrogen, and halogen atoms are added to another unsaturated carbon atom to obtain halogenated olefins or halogenated alkanes. Its alkynyl groups can also undergo nucleophilic addition, and nucleophilic reagents attack alkynyl carbon atoms to form new carbon-heteroatom bonds, forming complex structures in organic synthesis.

The hydroxyl group properties of alcohols are also important, and substitution reactions can occur, such as reaction with phosphorus halide, the hydroxyl group is replaced by halogen atoms to generate halogenated hydrocarbons, which is a common method for preparing halogenated hydrocarbons; esterification reaction with carboxylic acids under acid catalysis forms ester compounds, which are widely used in the synthesis of fragrances and drugs. And hydroxyl groups can participate in the formation of intermolecular hydrogen bonds, which affect the physical properties of substances, such as boiling point and solubility. Due to hydrogen bonding, the boiling point of (2E) -4,4,4-trifluorobutyl-2-yne-1-ol is relatively high, and it has a certain solubility in polar solvents.

In addition, trifluoromethyl in the molecule has strong electron absorption, which affects the distribution of molecular electron clouds, alters the reactivity of alkynyl and hydroxyl groups, enhances the polarity of adjacent chemical bonds, and makes reactions more prone to occur. It also affects the stability and biological activity of substances. In drug development, trifluoromethyl compounds often exhibit special biological activities due to their unique properties.

What are the synthesis methods of (2E) -4,4,4-trifluorobutyl-2-ene-1-ol?

The synthesis of (diethyl) -4,4,4-trifluorobutyric acid-2-alkynyl-1-ol is a key research direction in the field of chemistry. There are many methods, which are described in detail in ancient Chinese.

First, the nucleophilic substitution reaction can be carried out through specific halogenated hydrocarbons and compounds containing alkynyl groups under suitable catalyst and basic conditions. Halogenated hydrocarbons carry specific structures such as trifluoromethyl, and interact with alkynyl anions of alkynyl alcohols in a mild reaction environment. Like yin and yang, the two are connected to form an intermediate product containing alkynyl groups. After further functional group conversion, alcohol hydroxyl groups are modified, or oxidation, esterification and other reactions are carried out to achieve the synthesis of the target product. This process requires fine control of the reaction conditions, such as temperature and catalyst dosage, just like riding a horse and driving a horse, and the scale must be checked, otherwise side reactions will easily occur and the product will be impure.

Second, take advantage of the special reactivity of fluorine-containing compounds. Using fluorine-containing carboxylic acid derivatives as the starting material, the carboxyl group is first converted into an alcohol hydroxyl group through a reduction reaction to obtain a fluorine-containing alcohol compound. After introducing the alkynyl group, the alkynyl group can be connected to the alcohol derivative under an appropriate catalytic system. This step is like threading a needle and requires precise operation. Subsequent fine-tuning of the molecular structure, such as adjusting the position and type of substituents, ensures that the product structure is correct.

Third, a cyclization reaction strategy can also be used. Design a multi-functional group precursor compound with a specific structure to undergo intramolecular cyclization reaction under suitable conditions. After cyclization, the basic skeleton is constructed, and then the required functional groups such as trifluoromethyl, alkynyl group and alcohol hydroxyl group are introduced through ring opening and functional group modification. This process is like building a castle. Every step requires careful planning, following the reaction mechanism, and making steady progress to successfully construct the complex structure of the target molecule.

All kinds of synthesis methods have their own advantages and disadvantages. Experimenters should make careful choices and use them flexibly according to actual situations, such as raw material availability, cost considerations, product purity requirements, etc., in order to achieve the purpose of synthesis.

What are the precautions for (2E) -4,4,4-trifluorobutyl-2-ene-1-ol during storage and transportation?

(2E) -4,4,4-trifluorobutyl-2-ene-1-ol should not be ignored during storage and transportation.

This substance is volatile and should be stored in a cool and ventilated warehouse. The temperature of the warehouse should be strictly controlled and should not be too high. It is easy to increase its volatilization due to high temperature, and even cause danger. And keep away from fire and heat sources. Many open flames and heating equipment should be kept at a safe distance, otherwise a little careless, in case of open flames or hot topics, it may ignite a raging fire and cause unpredictable disasters.

During transportation, there are also many precautions. Be sure to ensure that the container does not leak, collapse, fall, or damage. If the container is damaged, (2E) -4,4,4-trifluorobutyl-2-ene-1-ol leaks out, which will not only cause material loss, but also may pose a serious threat to the environment and the safety of transportation personnel. Vehicles used during transportation should be driven according to the specified route, and must not change the route at will. It is especially necessary to be cautious when passing through densely populated areas, in case of an accident that affects many innocent people.

At the same time, whether it is storage or transportation, it must be stored separately from oxidants, acids, alkalis and other substances, and must not be mixed. Because of its active chemical nature, contact with these substances is very likely to cause violent chemical reactions, causing explosions and other vicious accidents. The relevant operators also need to undergo specialized training to master the operating procedures. During the operation, they must strictly abide by various safety regulations and wear appropriate protective equipment, such as protective gloves and goggles, to ensure their own safety.