2 Trifluoromethyl 5 Fluorobenzylcyanide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Trifluoromethyl-5-fluorobenzylcyanide
Chemical Formula C9H5F4N
Molecular Weight 203.14
Chemical Formula C9H5F4N
Appearance Typically a colorless to pale - yellow liquid (description may vary based on purity)
Boiling Point Data specific to this compound needs to be sourced from chemical databases (no common - known value provided here)
Melting Point Data specific to this compound needs to be sourced from chemical databases (no common - known value provided here)
Density Data specific to this compound needs to be sourced from chemical databases (no common - known value provided here)
Solubility May have limited solubility in water, but likely more soluble in organic solvents like dichloromethane, ethyl acetate (qualitative prediction)
Vapor Pressure Data specific to this compound needs to be sourced from chemical databases (no common - known value provided here)
Flash Point Data specific to this compound needs to be sourced from chemical databases (no common - known value provided here)
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
FAQ

What is the chemistry of 2-Trifluoromethyl-5-fluorobenzylcyanide?

2-Trifluoromethyl-5-fluorobenzyl cyanide is one of the organic compounds. It has unique chemical properties and is of great significance to the field of organic synthesis.

In this compound, the presence of trifluoromethyl and fluorine atoms greatly affects its chemical properties. Trifluoromethyl, because of its strong electronegativity of fluorine atoms, confers a significant electron-absorbing effect on the compound. This effect can change the distribution of molecular electron clouds, affecting the reactivity and selectivity. Fluorine atoms also have similar effects, and due to their small radius, they can enhance molecular stability and change the physical and chemical properties of compounds.

In chemical reactions, the cyanyl group of 2-trifluoromethyl-5-fluorobenzyl cyanide has high activity. Cyanyl groups can participate in many reactions, such as hydrolysis reactions to generate corresponding carboxylic acids; or react with nucleophiles to form new carbon-carbon bonds and carbon-heteroatom bonds, which are key intermediates in multi-step reactions in organic synthesis.

Due to the special properties of fluorine-containing groups, 2-trifluoromethyl-5-fluorobenzyl cyanide has attracted much attention in the fields of pharmaceutical chemistry and materials science. In pharmaceutical chemistry, fluorinated organic compounds often have unique biological activities, such as better fat solubility and metabolic stability, which help to improve drug efficacy and pharmacokinetic properties. In the field of materials science, the introduction of fluorinated compounds can improve the surface properties, thermal stability and chemical stability of materials.

However, this compound also contains fluorine, and its synthesis and treatment require special methods and conditions. During the synthesis process, the selection of fluorinated reagents and the control of reaction conditions should be considered to ensure the efficient and selective reaction. At the same time, due to its chemical activity, safety must be paid attention to during storage and use to avoid accidental reactions caused by contact with active substances.

What are the common uses of 2-Trifluoromethyl-5-fluorobenzylcyanide?

2-Trifluoromethyl-5-fluorobenzyl cyanide is widely used in the field of organic synthesis.

First, it can be used as a pharmaceutical intermediate. The structure of fluorine and cyanyl groups gives it unique chemical and biological properties. In the process of drug development, it can be cleverly spliced with other compounds through specific reactions to build molecular structures with specific pharmacological activities. For example, in the creation of anti-cancer drugs, it may participate in the construction of key intermediates to help develop high-efficiency and low-toxicity anti-cancer new drugs.

Second, it is also highly valued in the field of pesticide synthesis. Fluorinated organic compounds often have good biological activity and stability. Pesticides such as insecticides and fungicides can be prepared from this substance as a starting material through a series of chemical transformations. Such pesticides often exhibit high selectivity and efficiency to target organisms, and due to structural characteristics, they have good degradation performance in the environment, which can reduce the negative impact on the environment.

Third, it also has potential uses in materials science. Its special functional groups can enable it to participate in the synthesis process of polymer materials. For example, polymerization with suitable monomers, or materials that can prepare polymers with special properties, such as high chemical stability and low surface energy, may have extraordinary application prospects in coatings, plastics and other industries.

Furthermore, in the study of organic synthesis chemistry, 2-trifluoromethyl-5-fluorobenzyl cyanide is often used as a key building block. With its unique functional groups, chemists can modify and expand its structure with the help of various classical organic reactions, such as nucleophilic substitution, addition reactions, etc., to synthesize complex and novel organic compounds, providing materials and bases for theoretical research and new substance creation in organic chemistry.

What is 2-Trifluoromethyl-5-fluorobenzylcyanide synthesis method?

The synthesis of 2-trifluoromethyl-5-fluorobenzyl cyanide is a key topic in organic synthetic chemistry. Its synthesis paths are diverse, often depending on the available raw materials, reaction conditions, and the purity and yield requirements of the target product.

The first synthesis is initiated by halogenated aromatics. Take 2-trifluoromethyl-5-fluorohalobenzene containing an appropriate halogen atom (such as bromine or chlorine), and a cyanide reagent, such as potassium cyanide or sodium cyanide, in an appropriate solvent (such as N, N-dimethylformamide), in the presence of a catalyst (such as cuprous iodide, etc.), through a nucleophilic substitution reaction, the halogen atom is replaced by a cyanyl group to form a target product precursor, and then through a subsequent benzylation reaction, with a suitable benzylation reagent (such as benzyl halides), under the action of a base (such as potassium carbonate), 2-trifluoromethyl-5-fluorobenzyl cyanide can be obtained. The conditions of this path are mild, but the reaction process and the ratio of reagents need to be carefully controlled to obtain a high-purity product.

Furthermore, with 2-trifluoromethyl-5-fluorobenzoic acid as the starting material, it is first converted into an acid chloride, which can be co-heated with thionyl chloride. The obtained acid chloride is then reacted with ammonia to form an amide, which is dehydrated under the action of a dehydrating agent (such as phosphorus pentoxide, etc.) to obtain 2-trifluoromethyl-5-fluorobenzyl cyanide. Although this process is slightly complicated, the reaction selectivity of each step is good, which helps to improve the purity of the product.

Another synthesis method using arylboronic acid derivatives as raw materials. 2-Trifluoromethyl-5-fluoroaryl boronic acid and halobenzonitrile derivatives, in the presence of palladium catalysts (such as tetra (triphenylphosphine) palladium, etc.) and bases (such as sodium carbonate), through Suzuki-Miyaura coupling reaction, the carbon-carbon bond of the target product is directly constructed. This reaction has the advantages of high atomic economy and relatively mild conditions.

When synthesizing 2-trifluoromethyl-5-fluorobenzyl cyanide, precise control of reaction conditions, such as temperature, reaction time, reagent concentration and dosage, is crucial. At the same time, the separation and purification of the product cannot be ignored, and column chromatography and recrystallization are often used to ensure the high purity of the product and meet the needs of subsequent applications.

What is the market price of 2-Trifluoromethyl-5-fluorobenzylcyanide?

What you are asking about is the market price of 2-trifluoromethyl-5-fluorobenzyl cyanide. However, the price of this chemical is difficult to generalize, and it varies due to many factors.

First, the state of supply and demand has a great impact on its price. If the demand for this product is strong and the supply is limited, if the downstream industry develops rapidly and the demand for it increases sharply, and the manufacturer fails to expand production capacity in time, the price will rise. On the contrary, if the market demand is low and the supply exceeds the demand, the price may decline.

Second, the price of raw materials is also key. The production of this chemical requires specific raw materials. If the price of raw materials fluctuates, its cost will be implicated. If raw materials are scarce or prices rise for some reason, the price of this chemical will also increase in order to ensure profits.

Third, the level of production costs is related to the price. The complexity of the production process, the difficulty of the required technology, the amount of energy consumption and labor costs are all factors in the production cost. If the production process is complex, high-end technology and a lot of energy consumption are required, and the cost increases, the price will also increase accordingly.

Fourth, the market competition situation has a significant impact. If there are many manufacturers producing this chemical in the market, the competition is fierce, and each manufacturer is competing for a share, it may attract customers with price advantages, resulting in lower prices. If the market is almost monopolized and only a few manufacturers control the production, the pricing power is strong and the price may be higher.

Fifth, the impact of policies and regulations should not be underestimated. The strictness of environmental protection policies will affect the cost of the production process. If environmental protection requirements are increased, manufacturers need to invest more funds in environmental protection treatment, and the cost will rise, and the price may be driven.

To sum up, in order to know the exact market price of 2-trifluoromethyl-5-fluorobenzyl cyanide, it is necessary to carefully observe market supply and demand, raw material prices, production costs, competition conditions, policies and regulations and many other factors, and need to pay attention to market dynamics in real time, in order to obtain more accurate price information.

2-Trifluoromethyl-5-fluorobenzylcyanide need to pay attention to when storing and transporting

2-Trifluoromethyl-5-fluorobenzyl cyanide is an organic chemical substance, and many points must be paid attention to when storing and transporting it.

Store first. This substance should be placed in a cool, dry and well-ventilated place. Because it is sensitive to heat, high temperature can easily cause chemical reactions such as decomposition, which endangers safety, so a cool environment is essential. Drying is also indispensable, and moisture can easily cause adverse reactions such as hydrolysis, which affects its quality and stability. Good ventilation can avoid the accumulation of volatile substances and reduce potential hazards. And should be stored separately from oxidants, acids, alkalis, etc. Contact with these substances is likely to trigger violent chemical reactions, such as oxidation-reduction reactions, acid-base neutralization reactions, etc., which not only damage the substance itself, but also may lead to serious consequences such as fire and explosion. At the same time, the storage area must be equipped with obvious warning signs to remind personnel of its danger, and should be equipped with corresponding emergency treatment equipment and protective equipment, such as fire extinguishers, eye washers, gas masks, etc., in order to deal with emergencies.

As for transportation. Before transportation, ensure that the packaging is intact, and the packaging materials used should be able to effectively resist vibration, collision and friction, to prevent the packaging from breaking and causing material leakage. During transportation, the temperature should be strictly controlled to avoid large fluctuations in temperature. Vehicles should be equipped with good ventilation equipment to discharge possible volatile gases in time. Transport personnel must be professionally trained to be familiar with the properties, hazards and emergency treatment methods of the substance. During transportation, close attention should also be paid to prevent sun and rain, and keep away from fire and heat sources. In the event of a leak, emergency measures should be taken immediately, evacuate the surrounding personnel, seal the site, and choose appropriate methods to deal with the leak according to the situation, such as adsorption with inert materials such as sand, and then properly collect and dispose of it. In this way, the safety of 2-trifluoromethyl-5-fluorobenzyl cyanide during storage and transportation can be ensured.