96134-01-9

Basic information

• Product Name: 4-methoxy-N'-thiocarbamoyl-benzohydrazonic acid ethyl ester
• CAS NO: 96134-01-9
• Molecular Weight: 253.325
• Mol File: 96134-01-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methoxy-N'-thiocarbamoyl-benzohydrazonic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-N'-thiocarbamoyl-benzohydrazonic acid ethyl ester(96134-01-9)
• EPA Substance Registry System: 4-methoxy-N'-thiocarbamoyl-benzohydrazonic acid ethyl ester(96134-01-9)

Safety Data

• Hazardous Substances Data: 96134-01-9(Hazardous Substances Data)

Upstream product

• 54998-29-7 ethyl 4-methoxybenzimidate hydrochloride 
• 79-19-6 thiosemicarbazide 
• 59118-33-1 1-methoxy-4-triethoxymethyl-benzene 

Downstream Products

• 22926-59-6 2,2,2-trifluoro-N-(5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl)acetamide 
• 461014-07-3 3-((5-(4-methoxyphenyl)-1,3,4-thiadiazol-2-yl)carbamoyl)propanoic acid 
• 96134-47-3 [3-(4-Methoxy-phenyl)-5-methylsulfanyl-[1,2,4]triazol-4-yl]-phenyl-amine 
• 96424-91-8 2-[3-(4-Methoxy-phenyl)-5-methylsulfanyl-[1,2,4]triazol-4-yl]-ethanol 
• 1014-25-1 5-(4-methoxy-phenyl)-[1,3,4]thiadiazol-2-ylamine 
• 23282-98-6 4-benzyl-5-(4-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 96134-15-5 5-(4-Methoxy-phenyl)-4-phenylamino-2,4-dihydro-[1,2,4]triazole-3-thione 
• 91759-68-1 5-(4-methoxyphenyl)-4-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 96134-09-7 4-(2-Hydroxy-ethyl)-5-(4-methoxy-phenyl)-2,4-dihydro-[1,2,4]triazole-3-thione 
• 33901-36-9 5-(4-methoxyphenyl)-2,4-dihydro-3H[1,2,4]triazole-3-thione 
• 103989-36-2 N-[(4-methoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-acetamide 
• 33901-36-9 5-(4-methoxy-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 96134-21-3 N-[3-(4-Methoxy-phenyl)-5-thioxo-1,5-dihydro-[1,2,4]triazol-4-yl]-benzamide 

Relevant articles and documents

Sulfamic acid-mediated, efficient, one-pot synthesis of novel 5-substituted 1,3,4-thiadiazol-2-ylcarbamoyl aliphatic amide acid derivatives and facile synthesis of cyclic amides

Convenient and efficient one-pot syntheses of 5-substituted-1,3,4- thiadiazol-2- ylcarbamoyl aliphatic amide acid derivatives were described and developed using sulfamic acid catalyst. Thiosemicarbazide and substituted triethylorthoester and cyclic/alicyc