162221-97-8

Basic information

• Product Name: 4-(4-bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl hydrosulfide
• Synonyms: 4-(4-bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl hydrosulfide
• CAS NO: 162221-97-8
• Molecular Formula: C₁₄H₁₀BrN₃S
• Molecular Weight: 332.2183
• Mol File: 162221-97-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(4-bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl hydrosulfide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl hydrosulfide(162221-97-8)
• EPA Substance Registry System: 4-(4-bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl hydrosulfide(162221-97-8)

Safety Data

• Hazardous Substances Data: 162221-97-8(Hazardous Substances Data)

Upstream product

• 38240-75-4 1-benzoyl-4-(4-bromophenyl)thiosemicarbazide 
• 1985-12-2 4-Bromophenyl isothiocyanate 
• 613-94-5 benzoic acid hydrazide 
• 100-52-7 benzaldehyde 
• 2646-31-3 4-(p-bromophenyl)thiosemicarbazide 

Downstream Products

• 1516888-34-8 4-(4-bromophenyl)-5-phenyl-3-(2,3,4,6-tetra-O-acetyl-β-D-1-thioglucopyranose)-1,2,4-triazole 
• 1516888-09-7 4-(4-bromophenyl)-5-phenyl-3-(2,3,4,6-tetra-O-acetyl-β-D-1-thiogalactopyranose)-1,2,4-triazole 
• 1326882-31-8 4-(4-bromophenyl)-2-(morpholin-4-ylmethyl)-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 1326830-45-8 4-(4-bromophenyl)-5-phenyl-2-(piperidin-1-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 1403137-21-2 4-(4-bromophenyl)-5-phenyl-2-(pyrrolidin-1-ylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 1403137-18-7 4-(4-bromophenyl)-2-[(diethylamino)methyl]-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione 

Relevant articles and documents

Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C-N Bond over C-S Bond Formation

The higher propensity of C-N over C-S bond forming ability was demonstrated, through formal C-H functionalization during the construction of 4,5-disubstituted 1,2,4-triazole-3-thiones from arylidenearylthiosemicarbazides catalyzed by Cu(II). However, ster

Synthesis of new 1,2,4-Triazole-5-thiones and their thioglycoside derivatives as potential antibacterial agents

Abstract The glycosylation of 1,2,4-triazole-5-thiones has been performed with peracetylated β-pyranosyl bromide in the presence of potassium carbonate. The synthesized compounds were tested for their antimicrobial activity against bacterial (Gram-negative and Gram-positive) and yeasts strains in vitro. The synthetic compounds showed different inhibition zones against tested bacterial and yeasts strains. Among them, compounds which possessed 2-furyl and p-bromophenyl moieties showed the best results against Acinetobacter calcoaceticus ATCC 23055.

Synthesis and tuberculostatic activity of some 2-piperazinmethylene derivatives 1,2,4-triazole-3-thiones

The Mannich reaction's products of 1,2,4-triazole-3-thiones, substituted in position 4 (with ethyl, allyl, phenyl, Ph-4-Br) or 5 (with phenyl, Ph-4-OH, Ph-3,4,5-(OMe)3, 2-phenyl) were obtained. Their amino-components were 1-phenylpiperazine, 1-