97555-70-9

Basic information

• Product Name: 1,2,4-Triazolo[4,3-b][1,2,4]triazine-3(2H)-thione, 6,7-diphenyl-
• CAS NO: 97555-70-9
• Molecular Formula: C16H11N5S
• Molecular Weight: 305.363
• Mol File: 97555-70-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2,4-Triazolo[4,3-b][1,2,4]triazine-3(2H)-thione, 6,7-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Triazolo[4,3-b][1,2,4]triazine-3(2H)-thione, 6,7-diphenyl-(97555-70-9)
• EPA Substance Registry System: 1,2,4-Triazolo[4,3-b][1,2,4]triazine-3(2H)-thione, 6,7-diphenyl-(97555-70-9)

Safety Data

• Hazardous Substances Data: 97555-70-9(Hazardous Substances Data)

Upstream product

• 3529-50-8 4,5-diamino-2,4-dihydro-[1,2,4]triazole-3-thione 
• 134-81-6 benzil 
• 21383-24-4 (5,6-diphenyl-[1,2,4]triazin-3-yl)-hydrazine 
• 622-78-6 Benzyl isothiocyanate 
• 103-72-0 phenyl isothiocyanate 
• 2131-55-7 4-Chlorophenyl isothiocyanate 
• 1122-82-3 isothiocyanatocyclohexane 
• 621-30-7 3-methylphenyl isothiocyanate 
• 1985-12-2 4-Bromophenyl isothiocyanate 
• 592-82-5 butyl isothiocyanate 
• 75-15-0 carbon disulfide 
• 28735-33-3 5,6-diphenyl-3-methylthio-1,2,4-triazine 
• 37469-24-2 5,6-diphenyl-1,2,4-triazine-3-thiol 
• 116441-21-5 N-(5,6-diphenyl-1,2,4-triazin-3-yl)-N'-hydrazine 

Downstream Products

• 1283693-38-8 C₂₂H₂₁N₅O₅S 
• 1283693-37-7 C₂₇H₂₅N₅O₇S 
• 1283693-35-5 C₃₀H₂₉N₅O₉S 

Relevant articles and documents

Synthesis and antitumor activity evaluation of some 1, 2, 4-triazine and fused triazine derivatives

Reactions of 3-hyrazino-5,6-diphenyl-1,2,4-triazine with various carbonyl compounds such as ethyl acetoacetate, acetylacetone, benzoin, isatin, phthalic anhydride, phenyl isocyanate and acetic anhydride were discussed. Its reactions with α, β unsaturated

Synthesis of Some Substituted Triazolotriazines as Potential Anticancer Agents

The synthesis of some 3-substituted amino-6,7-diphenyl-1,2,4-triazolotriazines (15) by cyclodesulfurisation of the corresponding N-(5,6-diphenyl-1,2,4-triazin-3-yl)-N'-hydrazines (3) using dicyclohexylcarbodiimi