914225-58-4 Usage
Description
4-Bromo-3-chloro-5-(trifluoromethyl)aniline is a halogenated aniline derivative with the molecular formula C7H4BrClF3N. It features an aromatic ring structure and the presence of a bromine, chlorine, and trifluoromethyl group attached to the aniline core. This versatile chemical is known for its potential toxicity and should be handled with caution. It has been the subject of research and development due to its unique structure and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
4-Bromo-3-chloro-5-(trifluoromethyl)aniline is used as an intermediate in the synthesis of pharmaceuticals for its unique structure and potential medicinal properties.
Used in Agrochemical Industry:
4-Bromo-3-chloro-5-(trifluoromethyl)aniline is used as a building block in the development of agrochemicals, contributing to the creation of effective and targeted products for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 914225-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 914225-58:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*5)+(2*5)+(1*8)=154
154 % 10 = 4
So 914225-58-4 is a valid CAS Registry Number.
914225-58-4Relevant articles and documents
Synthesis method of 2-(2, 2-difluoroethyoxyl)-6-trifluoromethyl benzenesulfonyl chloride
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, (2021/06/13)
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.