CAS 79213-76-6
:Methyl N-(6-mercapto-1H-benzimidazol-2-yl)carbamate
Description:
Methyl N-(6-mercapto-1H-benzimidazol-2-yl)carbamate, identified by its CAS number 79213-76-6, is a chemical compound that features a benzimidazole core substituted with a mercapto group and a carbamate moiety. This compound typically exhibits properties associated with both the benzimidazole and carbamate functional groups, such as potential biological activity and solubility in organic solvents. The presence of the mercapto group suggests that it may participate in redox reactions or form disulfide bonds, which can be significant in biological systems. Methyl N-(6-mercapto-1H-benzimidazol-2-yl)carbamate may also exhibit antimicrobial or antifungal properties, making it of interest in pharmaceutical applications. Its molecular structure allows for interactions with various biological targets, and it may be studied for its potential therapeutic effects. As with many chemical substances, safety data and handling precautions should be observed, given the presence of sulfur and nitrogen in its structure, which can influence its reactivity and toxicity.
Formula:C9H9N3O2S
InChI:InChI=1S/C9H9N3O2S/c1-14-9(13)12-8-10-6-3-2-5(15)4-7(6)11-8/h2-4,15H,1H3,(H2,10,11,12,13)
InChI key:InChIKey=KXPVTEAMOUVXHO-UHFFFAOYSA-N
SMILES:N(C(OC)=O)C=1NC=2C(N1)=CC=C(S)C2
Synonyms:- 2-[(Methoxycarbonyl)amino]-5-benzimidazolethiol
- Carbamic acid, (5-mercapto-1H-benzimidazol-2-yl)-, methyl ester
- Carbamicacid, (5-mercapto-1H-benzimidazol-2-yl)-, methyl ester (9CI)
- Methyl N-(6-mercapto-1H-benzimidazol-2-yl)carbamate
- Carbamic acid, N-(6-mercapto-1H-benzimidazol-2-yl)-, methyl ester
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