7382-39-0

Basic information

• Product Name: Hydrazinecarbothioamide, 2-(4-methoxyphenyl)-
• CAS NO: 7382-39-0
• Molecular Formula: C8H11N3OS
• Molecular Weight: 197.261
• Mol File: 7382-39-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Hydrazinecarbothioamide, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarbothioamide, 2-(4-methoxyphenyl)-(7382-39-0)
• EPA Substance Registry System: Hydrazinecarbothioamide, 2-(4-methoxyphenyl)-(7382-39-0)

Safety Data

• Hazardous Substances Data: 7382-39-0(Hazardous Substances Data)

Upstream product

• 2284-20-0 4-Methoxyphenyl isothiocyanate 
• 104-94-9 4-methoxy-aniline 
• 1142816-82-7 C₈H₈NOS₂^(1-)*K⁽¹⁺⁾ 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 1147550-11-5 ammonium thiocyanate 
• 3471-32-7 4-Methoxyphenylhydrazine 

Downstream Products

• 908827-82-7 2′-benzoylpyridine 4-(p-methoxyphenyl)-3-thiosemicarbazone 
• 78559-93-0 N'-[4-(4-bromophenyl)thiazol-2-yl]-N-(4-methoxybenzylidene)hydrazine 
• 94672-28-3 N,N'-bis(4-methoxyphenyl)hydrazine-1,2-bis(carbothioamide) 
• 1220213-35-3 1-(4-methoxyphenyl)-3-(methylsulfonyl)-5-(4-(methylsulfonyl)phenyl)-1H-1,2,4-triazole 
• 1220213-25-1 1-(4-methoxyphenyl)-3-(methylsulfinyl)-5-(4-(methylsulfonyl)phenyl)-1H-1,2,4-triazole 
• 1220213-42-2 4-(1-(4-methoxyphenyl)-3-(methylthio)-1H-1,2,4-triazol-5-yl)benzenesulfonamide 
• 1220213-58-0 C₂₀H₂₄N₄O₃S₂ 
• 1220213-16-0 1-(4-methoxyphenyl)-5-(4-(methylsulfonyl)phenyl)-3-(methylthio)-1H-1,2,4-triazole 
• 1220213-56-8 C₁₉H₂₂N₄O₃S₂ 
• 1254037-59-6 C₁₆H₁₅N₃O₃S₂ 
• 68337-52-0 1-(4-methoxy-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 99793-13-2 1,5-bis(4-methoxyphenyl)-3-(methylthio)-1H-1,2,4-triazole 
• 100781-49-5 1,5-Bis-(4-methoxy-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 65078-24-2 thiazolidin-2-one (4-methoxy-phenyl)-hydrazone 

Relevant articles and documents

the Golden Method : Electrochemical Synthesis Is an Efficient Route to Gold Complexes

Gold compounds to be obtained by the direct electrochemical oxidation of a noble metal are reported. This achievement provides an alternative procedure to obtaining neutral gold compounds with potential medical or catalytic applications.

Triazole derivatives

A compound of the formula (I): wherein R1 is lower alkyl which is optionally substituted with halogen, cyano, N,N-di(lower)alkylcarbamoyl, phenyl optionally substituted with halogen, or heterocyclic group, cyclo(lower)alkyl, lower alkynyl, or N