432-21-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-6-chlorobenzotrifluoride is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Amino-6-chlorobenzotrifluoride serves as an essential building block for the creation of new agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection, thereby supporting agricultural productivity.
Used in Dye Industry:
2-Amino-6-chlorobenzotrifluoride is utilized as a precursor in the production of dyes. Its chemical properties enable the creation of dyes with specific color characteristics and improved performance, catering to the diverse needs of various industries that rely on coloring agents.
Used in Polymer Industry:
As a building block in the production of polyfluoroarylene polymers, 2-Amino-6-chlorobenzotrifluoride contributes to the development of high-performance polymers with exceptional properties such as heat resistance, chemical stability, and electrical insulation. These polymers find applications in various sectors, including aerospace, electronics, and automotive industries.
Overall, 2-Amino-6-chlorobenzotrifluoride's versatility and unique chemical characteristics make it an indispensable component in the synthesis of a wide range of products across different industries, highlighting its importance as a chemical intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 432-21-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 432-21:
(5*4)+(4*3)+(3*2)+(2*2)+(1*1)=43
43 % 10 = 3
So 432-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClF3N/c8-4-2-1-3-5(12)6(4)7(9,10)11/h1-3H,12H2
432-21-3Relevant articles and documents
7-(4-(4-[3-CHLORO-2-(TRIFLUOROMETHYL)PHENYL]PIPERAZIN-1-YL)BUTOXY)-[1,8]-NAPHTHYRIDIN-2(1H)-ONE
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Page/Page column 4, (2008/12/06)
This invention relates to a compound of formula (I) or pharmaceutically acceptable salts thereof, pharmaceutical compositions containing the compound or a salt thereof, and its use as a medicament for the treatment of schizophrenia, bipolar disorder, or other central nervous system disorders.
Reactions of Trifluoromethyl Bromide and Related Halides: Part 10. Perfluoroalkylation of Aromatic Compounds induced by Sulphur Dioxide Radical Anion Precursors
Tordeux, Marc,Langlois, Bernard,Wakselman, Claude
, p. 2293 - 2299 (2007/10/02)
Perfluoroalkylation of electron-rich aromatic compounds with trifluoromethyl bromide, or long-chain perfluoroalkyl iodides, was performed in the presence of sodium dithionite or zinc-sulphur dioxide.This alkylation occurred at the ortho and para positions relative to the amino or hydroxy substitutent.Pyrroles were perfluoroalkylated regioselectively at the 2-position.This alkylation was interpreted as a radical aromatic substitution; the formation of the perfluoroalkyl radical can be induced by a single-electron transfer from sulphur dioxide radical anion to the perfluoroalkyl halide.
