122503-09-7

Basic information

• Product Name: BUTTPARK 58\40-23
• Synonyms: BUTTPARK 58\40-23;4-Amino-5-(1H-1,2,3-benzotriazol-1-ylmethyl)-4H-1,2,4-triazole-3-thiol;4-amino-5-(1-benzotriazolylmethyl)-2H-1,2,4-triazole-3-thione;4-amino-5-(benzotriazol-1-ylmethyl)-2H-1,2,4-triazole-3-thione;AO-476/41839747;ZINC00383362;ZINC02355145
• CAS NO: 122503-09-7
• Molecular Formula: C₉H₉N₇S
• Molecular Weight: 247.28
• Mol File: 122503-09-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BUTTPARK 58\40-23(CAS DataBase Reference)
• NIST Chemistry Reference: BUTTPARK 58\40-23(122503-09-7)
• EPA Substance Registry System: BUTTPARK 58\40-23(122503-09-7)

Safety Data

• Hazardous Substances Data: 122503-09-7(Hazardous Substances Data)

Upstream product

• 4144-64-3 2-(1H-1,2,3-benzotriazol-1-yl)acetic acid 
• 2231-57-4 Thiocarbohydrazide 

Downstream Products

• 122503-12-2 6-benzyl-3-<1-(1H-benzotriazole)methyl>-1,2,4-triazolo<3,4-b><1,3,4>thiadiazole 
• 122503-18-8 6-p-tolyl-3-<1-(1H-benzotriazole)methyl>-7H-1,2,4-triazolo<3,4-b><1,3,4>thiadiazine 
• 122503-13-3 6-phenyl-3-<1-(1H-benzotriazole)methyl>-1,2,4-triazolo<3,4-b><1,3,4>thiadiazole 
• 122503-19-9 6-p-methoxyphenyl-3-<1-(1H-benzotriazole)methyl>-7H-1,2,4-triazolo<3,4-b><1,3,4>thiadiazine 
• 825604-65-7 C₁₄H₉N₇OS 
• 1070666-55-5 C₁₆H₁₂N₈O₂S 
• 1070666-70-4 C₁₇H₁₅N₇S 
• 1070666-48-6 C₁₆H₁₂BrN₇S 
• 1070666-61-3 C₁₇H₁₅N₇OS 
• 1070666-64-6 C₁₇H₁₅N₇OS 
• 1070666-68-0 C₁₇H₁₅N₇S 
• 1070666-53-3 C₁₆H₁₂BrN₇S 
• 1070666-44-2 C₁₆H₁₂ClN₇S 
• 1070666-66-8 C₁₇H₁₅N₇OS 

Relevant articles and documents

Synthesis and cytotoxicity activity of novel benzotrizolyl methyl[1,2,4-triazolo][3,4-b]thiadiazinyl substituted chromene 2-ones

The biological importance of the coumarins and triazolothiadiazines, prompted as to synthesize a series of novel benzotrizolyl methyl[1,2,4-triazolo][3,4-b]thiadiazinyl substituted chromene 2-ones applying simple experimental conditions with good yields. All the synthesized molecules were well characterized by physical, analytical and spectroscopic techniques. The novel synthesized molecules 5(a-k) were screened for the anticancer activity and some of the molecules exhibited moderate to good activity in vitro.