5-Methoxy-2-mercaptobenzimidazole

CAS : 37052-78-1

Ref. 3D-FM00167

Informations sur le produit

• Nom: 5-Methoxy-2-mercaptobenzimidazole
• Synonymes: 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, 2-Mercapto-5-methoxybenzimidazole

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.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 180.23 g/mol
• Formule: C₈H₈N₂OS
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: 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)
• Code InChI: InChIKey=KOFBRZWVWJCLGM-UHFFFAOYSA-N
• SMILES: COc1ccc2[nH]c(=S)[nH]c2c1