1316270-44-6

Basic information

• Product Name: C₂₁H₁₅N₇O₂S
• CAS NO: 1316270-44-6
• Molecular Weight: 429.462
• Mol File: 1316270-44-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₂₁H₁₅N₇O₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₁H₁₅N₇O₂S(1316270-44-6)
• EPA Substance Registry System: C₂₁H₁₅N₇O₂S(1316270-44-6)

Safety Data

• Hazardous Substances Data: 1316270-44-6(Hazardous Substances Data)

Upstream product

• 95-53-4 o-toluidine 
• 20174-68-9 4-methyl-2-hydrazinobenzothiazole 
• 56352-95-5 2-(4-nitrophenyl)-5-(3-pyridinyl)-1,3,4-oxadiazole 
• 1477-42-5 4-methyl-1,3-benzothiazol-2-amine 
• 614-18-6 3-pyridinecarboxylic acid ethyl ester 
• 553-53-7 Nicotinic acid hydrazide 

Relevant articles and documents

Anti-HIV, antimycobacterial and antimicrobial studies of newly synthesized 1,2,4-triazole clubbed benzothiazoles

In an attempt to synthesize pharmacologically active molecules, we report here the synthesis and in vitro anti-HIV, antimycobacterial and antimicrobial activity of various series of 3-(3-pyridyl)-5-(4-substitutedphenyl)-4-(N- substituted-1,3-benzothiazol-2-amino)-4H-1,2,4-triazole. The anti-HIV activity of the title compounds was evaluated as selective human immunodeficiency virus type-1 and -2 (HIV-1, HIV-2 RT) inhibitors, antitubercular activity against H37Rv using Lowenstein-Jensen agar method and antimicrobial activity against certain bacterial and fungal strains using the broth microdilution method. The synthesized compounds were characterized by FTIR, 1H-NMR,13C-NMR and mass spectral data together with elemental analysis.