62827-39-8 Usage
Uses
Used in Pharmaceutical Industry:
5-AMINO1-BROMO-2-METHYL-3-NITROBENZENE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence of nitro and amino groups allows for the creation of a wide range of drug molecules, contributing to the development of new medications for treating various diseases and conditions.
Used in Dye Industry:
In the dye industry, 5-AMINO1-BROMO-2-METHYL-3-NITROBENZENE is utilized as a precursor for the production of dyes. Its chemical structure enables the creation of dyes with specific color properties, which are essential for various applications such as textiles, printing, and other industrial processes.
Used in Chemical Research:
5-AMINO1-BROMO-2-METHYL-3-NITROBENZENE is employed as a research compound in chemical laboratories. Its unique properties make it a valuable tool for studying chemical reactions and exploring new synthetic pathways, furthering the understanding of organic chemistry and its applications.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 5-AMINO1-BROMO-2-METHYL-3-NITROBENZENE is used to produce a variety of organic compounds. Its functional groups facilitate the formation of new chemical bonds, enabling the synthesis of complex molecules for use in various industries, including pharmaceuticals, materials science, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 62827-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,2 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62827-39:
(7*6)+(6*2)+(5*8)+(4*2)+(3*7)+(2*3)+(1*9)=138
138 % 10 = 8
So 62827-39-8 is a valid CAS Registry Number.
62827-39-8Relevant academic research and scientific papers
Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Part XXXIX - Reaction of 2-Mercapto-4-bromo-6-methylbenzimidazole with Chloroacetic Acid and 1,2-Dibromoethane
Jain, K. K.,Pujari, H. K.
, p. 294 - 295 (2007/10/02)
8-Bromo-6-methylthiazolobenzimidazol-3(2H)-one (IVa) and 8-bromo-6-methyl-2,3-dihydrothiazolobenzimidazole (V) have been synthesized starting from 2-mercapto-4-bromo-6-methylbenzimidazole (II), prepared by the reaction of 3-bromo-5-methyl-1,
