403646-45-7 Usage
Uses
Used in Pharmaceutical Industry:
3-Bromo-2-(trifluoromethoxy)benzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its potential application in anti-cancer drugs. Its unique chemical structure contributes to the development of new medicinal compounds with enhanced therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-2-(trifluoromethoxy)benzoic acid serves as an essential intermediate in the production of agrochemicals, aiding in the development of more effective and targeted pest control solutions.
Used in Dye and Pigment Manufacturing:
3-Bromo-2-(trifluoromethoxy)benzoic acid is utilized as a raw material in the manufacturing of dyes and pigments, contributing to the creation of a diverse range of colorants for various applications.
Used in Organic Compound Synthesis:
3-BROMO-2-(TRIFLUOROMETHOXY)BENZOIC ACID is employed as a versatile building block in the synthesis of other organic compounds, expanding its applications across different industries and contributing to the development of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 403646-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,6,4 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 403646-45:
(8*4)+(7*0)+(6*3)+(5*6)+(4*4)+(3*6)+(2*4)+(1*5)=127
127 % 10 = 7
So 403646-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrF3O3/c9-5-3-1-2-4(7(13)14)6(5)15-8(10,11)12/h1-3H,(H,13,14)
403646-45-7Relevant articles and documents
INDAZOLES AND AZAINDAZOLES AS LRRK2 INHIBITORS
-
Page/Page column 345; 346, (2021/01/29)
The present invention is directed to indazole and azaindazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS disorders.
1,2-Didehydro-3- and -4-(trifluoromethoxy)benzene: The "aryne" route to 1- and 2-(trifluoromethoxy)naphthalenes
Schlosser, Manfred,Castagnetti
, p. 3991 - 3997 (2007/10/03)
Upon treatment of 1-bromo-2-(trifluoromethoxy)benzene with lithium diisopropylamide (LIDA) at -100°C, 3-bromo-2-(trifluoromethoxy)phenyllithium is generated. It can be trapped as such, but isomerizes to afford 2-bromo-6-(trifluoromethoxy)phenyllithium whe