5-Methoxy-2-mercaptobenzimidazole

CAS: 37052-78-1

Ref. 3D-FM00167

Product Information

• Name: 5-Methoxy-2-mercaptobenzimidazole
• Synonyms: 1,3-Dihydro-5-methoxybenzimidazole-2-thione, 1,3-dihydro-5-methoxy-2H-benzimidazole-2-thione, 2-Mercapto-5-Methoxy Benzimidazole, 2-Mercapto-5-Methoxy-1H-Benzimidazole, 2-Thio-5-methoxy-1H-benzimidazole, 2H-Benzimidazole-2-thione, 1,3-dihydro-5-methoxy-, 5-Methoxy-1,3-Dihydro-Benzoimidazole-2-Thione, 5-Methoxy-1,3-dihydro-benzimidazol-2-thion, 5-Methoxy-1H-Benzo[D]Imidazole-2-Thiol, 5-Methoxy-1H-benzo[d]imidazole-2(3H)-thione, 5-Methoxy-1H-benzoimidazole-2-thiol, 5-Methoxy-2-Thiobenzimidazole, 5-Methoxy-2-benzimidazolethiol, 5-Methoxy-2-mercaplobenzinidazole, 5-Methoxy-2-mercapto-1H-benzimidazole, 5-Methoxybenzimidazole-2-thiol, 5-Methoxybenzimidazolin-2-Mercapto, 5-Methoxybenzimidazolin-2-Thione, 5-methoxy-1H-benzimidazole-2-thiol, 5-methyoxy-2-mercapto Benzimidazole, Esomeprazole EP impurities, Methoxy-2-mercaptobenzimidazole,5-, Timtec-Bb Sbb000219
• CAS: 37052-78-1

Description

5-Methoxy-2-mercaptobenzimidazole is a chiral compound that can be used as a reagent for the preparation of phosphate buffer. It reacts with tyrosinase to form a yellow product and phosphotungstic acid. The reaction solution contains sodium citrate, which is used to adjust the pH. 5-Methoxy-2-mercaptobenzimidazole is a benzimidazole derivative and its protonated form has an affinity for hydrogen bond formation. The magnesium salt in this reaction solution acts as an organic solvent. This analytical method has detection sensitivity at 10 ppm.

• Brand: Biosynth

Chemical properties

• Molecular weight: 180.23 g/mol
• Formula: C₈H₈N₂OS
• Purity: Min. 98 Area-%
• Color/Form: Powder
• InChI: InChI=1S/C8H8N2OS/c1-11-5-2-3-6-7(4-5)10-8(12)9-6/h2-4H,1H3,(H2,9,10,12)
• InChI key: InChIKey=KOFBRZWVWJCLGM-UHFFFAOYSA-N
• SMILES: COc1ccc2[nH]c(=S)[nH]c2c1