cas 455-24-3|| where to buy 4-(trifluoromethyl)benzoic acid

Product Name:4-(trifluoromethyl)benzoic acid

IUPAC Name:4-(trifluoromethyl)benzoic acid

: CAS：455-24-3; Molecular Formula：C8H5F3O2; Purity：95%+

: Catalog Number：CM101893; Molecular Weight：190.12

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Product Details

: CAS NO:455-24-3; Molecular Formula:C8H5F3O2; Melting Point:-; Smiles Code:O=C(O)C1=CC=C(C(F)(F)F)C=C1; Density:1.403 g/cm3

: Catalog Number:CM101893; Molecular Weight:190.12; Boiling Point:243.2°C at 760 mmHg; MDL No:MFCD00002562; Storage:Store at room temperature.

Category Infos

: Benzenes; Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos

: Carbonyl Compounds; In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes, ketones and carboxylic acids), as part of many larger functional groups. A compound containing a carbonyl group is often referred to as a carbonyl compound.

: Benzenes

Product Other Information

Product Overview	4-(trifluoromethyl)benzoic acid (4-TFMBA) is a versatile and important organic compound that has been studied extensively in the scientific community. It is an aromatic acid, containing a trifluoromethyl group at the fourth position of the benzene ring. 4-TFMBA has been used in a variety of scientific applications, including drug synthesis and research, as well as in laboratory experiments.
Synthesis and Application	The synthesis of 4-(trifluoromethyl)benzoic acid can be achieved through several different methods. One of the most common methods is the Friedel-Crafts alkylation reaction. This reaction involves the use of an alkyl halide, such as trifluoromethyl bromide, and a Lewis acid, such as aluminum chloride, to alkylate a benzene ring. The reaction is typically conducted in a solvent such as dichloromethane or toluene. Another method for the synthesis of 4-(trifluoromethyl)benzoic acid is the Knoevenagel condensation reaction. This reaction involves the condensation of an aldehyde or ketone with an aromatic acid, such as 4-(trifluoromethyl)benzoic acid, in the presence of a base, such as pyridine or sodium hydroxide. 4-(trifluoromethyl)benzoic acid has been used in a variety of scientific research applications. It has been used as a reagent in the synthesis of pharmaceuticals, such as antibiotics and anti-inflammatory drugs. It has also been used to synthesize organic compounds with potential therapeutic applications, such as antifungal agents and anticancer agents. In addition, 4-(trifluoromethyl)benzoic acid has been used as an intermediate in the synthesis of other organic compounds, such as dyes and fragrances.
Future Directions	There are many possible future directions for research on 4-(trifluoromethyl)benzoic acid. For example, further research could be conducted on the biochemical and physiological effects of 4-(trifluoromethyl)benzoic acid, as well as its potential therapeutic applications. In addition, further research could be conducted on the mechanism of action of 4-(trifluoromethyl)benzoic acid and its interactions with other molecules, such as proteins. Finally, further research could be conducted on the synthesis of 4-(trifluoromethyl)benzoic acid and the development of new methods for its synthesis.