835-14-3

Basic information

• Product Name: N₂-(2-nitrobenzoyl)thiosemicarbazide
• Synonyms: N₂-(2-nitrobenzoyl)thiosemicarbazide
• CAS NO: 835-14-3
• Molecular Weight: 240.243
• Mol File: 835-14-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N₂-(2-nitrobenzoyl)thiosemicarbazide(CAS DataBase Reference)
• NIST Chemistry Reference: N₂-(2-nitrobenzoyl)thiosemicarbazide(835-14-3)
• EPA Substance Registry System: N₂-(2-nitrobenzoyl)thiosemicarbazide(835-14-3)

Safety Data

• Hazardous Substances Data: 835-14-3(Hazardous Substances Data)

Upstream product

• 333-20-0 potassium thioacyanate 
• 606-26-8 o-nitrobenzohydrazide 
• 552-16-9 ortho-nitrobenzoic acid 
• 79-19-6 thiosemicarbazide 
• 610-14-0 2-nitrobenzyl chloride 
• 2290-65-5 trimethylsilyl isothiocyanate 

Downstream Products

• 832-79-1 5-(2-nitrophenyl)-1,3,4-thiadiazol-2-amine 
• 6219-49-4 5-(2-nitro-phenyl)-2,4-dihydro-[1,2,4]triazole-3-thione 
• 109060-71-1 2-amino-5-(2'-nitrophenyl)-1,3,4-oxadiazole 
• 1383783-63-8 4-(2-{[5-(2-nitrophenyl)-4H-1,2,4-triazol-3-yl]thio}ethoxy)benzaldehyde 
• 6219-49-4 3-(o-nitrophenyl)-5-mercapto-4H-1,2,4-triazole 
• 1173-99-5 4-acetylamino-N-[5-(2-nitro-phenyl)-[1,3,4]thiadiazol-2-yl]-benzenesulfonamide 
• 978-34-7 4-amino-N-[5-(2-nitro-phenyl)-[1,3,4]thiadiazol-2-yl]-benzenesulfonamide 
• 83543-30-0 α-(5-o-nitrophenyl-1,3,4-thiadiazol-2-yl-amino)-(3,5-dibromo-2-hydroxyphenyl)acetonitrile 
• 83530-83-0 α-(5-o-nitrophenyl-1,3,4-thiadiazol-2-yl-amino)-(5-bromo-4-hydroxy-3-methoxyphenyl)acetonitrile 

Relevant articles and documents

Mild and convenient one-pot synthesis of 2-amino-1,3,4-oxadiazoles promoted by trimethylsilyl isothiocyanate (TMSNCS)

A mild, convenient, and efficient one-pot synthesis of amino-1,3,4- oxadiazoles is described. In situ preparation of various thiosemicarbazides by the reaction of different carboxylic acid hydrazides with trimethylsilyl isothiocyanate (TMSNCS), followed by cyclodesulfurization of thiosemicarbazides under basic conditions in the presence of I2/KI resulted in 2-amino-1,3,4-oxadiazoles in high yields (79-94%).

Synthesis and evaluation of bioactivity of thiazolo[3,2-b]-[1,2,4]- triazoles and isomeric thiazolo[2,3-c]-[1,2,4]-triazoles

Synthesis of 2-(o-nitrophenyl)-6-arylthiazolo[3,2-b]-[1,2,4]-triazoles 4 and its isomer 3-(o-nitrophenyl)-5-arylthiazolo[2,3-c]-[1,2,4]-triazoles 6 has been achieved starting from the appropriate 1-(o-nitrobenzoyl)-3- thiosemicarbazide 1. Compound 1 on co

Synthesis of some 2 arylideneamino 5 aryl 1,3,4 thiadiazoles as potential fungicides

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