134832-82-9

Basic information

• Product Name: C₁₅H₁₄ClN₃OS₂
• CAS NO: 134832-82-9
• Molecular Weight: 351.881
• Mol File: 134832-82-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₄ClN₃OS₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₄ClN₃OS₂(134832-82-9)
• EPA Substance Registry System: C₁₅H₁₄ClN₃OS₂(134832-82-9)

Safety Data

• Hazardous Substances Data: 134832-82-9(Hazardous Substances Data)

Upstream product

• 90006-99-8 Hydrazin-monothiocarbonsaeure-S-benzylester 
• 2131-55-7 4-Chlorophenyl isothiocyanate 
• 100-44-7 benzyl chloride 

Downstream Products

• 134832-78-3 5-Benzylsulfanyl-4-(4-chloro-phenyl)-4H-[1,2,4]triazol-3-ol 
• 89894-23-5 4-(4-Chloro-phenyl)-5-mercapto-4H-[1,2,4]triazol-3-ol 

Relevant articles and documents

Thiocarbazinic acids: Interaction of carbonoxysulphide with thiosemicarbazides - Synthesis of &β-(thiocarbamyl)thiocarbazinates and 1,3,4-oxadiazole and 1,2,4-triazole derivatives

Interaction of carbon oxysulphide with 4-alkyl/arylthiosemicarbazides (I) in ethanol in the presence of sodium hydroxide forms sodium β-(N-alkyl/arylthiocarbamyl)thiocarbazinates (II).Benzylation of the latter (II) affords 5-alkyl/arylamino-2-benzylmercapto-1,3,4-oxadiazoles (IV), which can also be obtained by a one-pot synthesis involving the reaction of I with carbon oxysulphide in DMF in the presence of triethylamine and benzyl chloride.The syntheses of benzyl β-(N-alkyl/arylthiocarbamyl)thiocarbazinates (III) and 4-aryl-3-mercapto-1,2,4-triazolin-5-ones (VII) are also reported.Some of the compounds exhibit antibacterial activity.