914225-58-4

Basic information

• Product Name: 4-BROMO-3-CHLORO-5-(TRIFLUOROMETHYL)ANILINE
• Synonyms: 4-BROMO-3-CHLORO-5-(TRIFLUOROMETHYL)ANILINE;4-bromo-3-chloro-5-(trifluoromethyl)Benzenamine
• CAS NO: 914225-58-4
• Molecular Formula: C₇H₄BrClF₃N
• Molecular Weight: 274.4655696
• Mol File: 914225-58-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-BROMO-3-CHLORO-5-(TRIFLUOROMETHYL)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3-CHLORO-5-(TRIFLUOROMETHYL)ANILINE(914225-58-4)
• EPA Substance Registry System: 4-BROMO-3-CHLORO-5-(TRIFLUOROMETHYL)ANILINE(914225-58-4)

Safety Data

• Hazardous Substances Data: 914225-58-4(Hazardous Substances Data)

Usage

General Description

4-Bromo-3-chloro-5-(trifluoromethyl)aniline is a chemical compound with the molecular formula C7H4BrClF3N. It is a halogenated aniline derivative that is used in the synthesis of pharmaceuticals and agrochemicals. 4-Bromo-3-chloro-5-(trifluoromethyl)aniline is characterized by its aromatic ring structure and the presence of a bromine, chlorine, and trifluoromethyl group attached to the aniline core. It is also known for its potential toxicity and should be handled with caution. Additionally, it has been the subject of research and development due to its unique structure and potential applications in various industries. Overall, 4-Bromo-3-chloro-5-(trifluoromethyl)aniline is a versatile chemical with potential uses in medicinal and agricultural fields.

Upstream product

• 367-67-9 2-bromo-5-nitro-benzotrifluoride 
• 69411-05-8 3-chloro-5-(trifluoromethyl)phenylaniline 

Downstream Products

• 865352-01-8 2-(2',2'-difluoroethoxy)-6-trifluoromethylbenzene-1-sulfonyl chloride 
• 384-16-7 2-bromo-1-chloro-3-(trifluoromethyl)benzene 
• 1533424-29-1 N³-(4-bromo-3-chloro-5-(trifluoromethyl)phenyl)-1H-1,2,4-triazole-3,5-diamine 
• 1533434-96-6 (Z)-methyl N-(4-bromo-3-chloro-5-(trifluoromethyl)phenyl)-N'-cyanocarbamimidothioate 
• 1533425-20-5 2-bromo-1-chloro-5-isothiocyanato-3-(trifluoromethyl)benzene 

Relevant articles and documents

Synthesis method of 2-(2, 2-difluoroethyoxyl)-6-trifluoromethyl benzenesulfonyl chloride

The invention discloses a synthesis method of 2-(2, 2-difluoroethyoxyl)-6-trifluoromethyl benzenesulfonyl chloride. The preparation method comprises the following steps: dissolving 2-trifluoromethyl-4-nitro-bromobenzene in sulfuric acid, adding a halogenating reagent, and reacting at 50-100 DEG C for 1-8 hours; dissolving the obtained 2-bromo-3-trifluoromethyl-5-nitro-benzene halide in a solvent, and performing reduction in a reduction system; carrying out diazotization on the obtained 3-halo-4-bromo-5-trifluoromethyl-aniline, and then carrying out decomposition on the obtained 3-halo-4-bromo-5-trifluoromethyl-aniline; carrying out Grignard reaction on the obtained 2-bromo-3-trifluoromethyl-benzene halide, and then reacting with dialkyl disulfide; carrying out etherification reaction on the obtained 2-alkylthio-3-trifluorotoluene-benzene halide and 2, 2-difluoroethanol in an organic solvent under the action of an alkali; and reacting the obtained 2-(2, 2-difluoroethoxy)-6-trifluoromethyl-phenylalkyl sulfide with chlorine gas at 10-60 DEG C for 1-5 hours. The method is short in route, mild in condition, high in yield and suitable for industrial production.