61733-82-2

Basic information

• Product Name: Acetic acid, 2-[(phenylamino)carbonyl]hydrazide
• CAS NO: 61733-82-2
• Molecular Formula: C9H11N3O2
• Molecular Weight: 193.205
• Mol File: 61733-82-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Acetic acid, 2-[(phenylamino)carbonyl]hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, 2-[(phenylamino)carbonyl]hydrazide(61733-82-2)
• EPA Substance Registry System: Acetic acid, 2-[(phenylamino)carbonyl]hydrazide(61733-82-2)

Safety Data

• Hazardous Substances Data: 61733-82-2(Hazardous Substances Data)

Upstream product

• 1068-57-1 acetic acid hydrazide 
• 67-64-1 acetone 
• 582-61-6 benzoyl azide 
• 141-78-6 ethyl acetate 
• 537-47-3 4-phenyl-semicarbazide 
• 103-71-9 phenyl isocyanate 
• 108-24-7 acetic anhydride 

Downstream Products

• 537-47-3 4-phenyl-semicarbazide 
• 64-19-7 acetic acid 
• 105008-05-7 Co(CH₃CONHNHCONHC₆H₅)Cl₂(H₂O)*H₂O 
• 105008-06-8 Co(CH₃CONHNHCONHC₆H₅)(CH₃COO)2 
• 105029-96-7 Cu₂(CH₃CONHNHCONHC₆H₅)Br₂ 
• 105008-07-9 Ni(CH₃CONHNHCONHC₆H₅)Cl₂ 
• 105008-10-4 Cu₂(CH₃CONHNHCONHC₆H₅)Cl₂ 
• 1969-09-1 N-phenyl-(5-methyl-[1,3,4]oxadiazol-2-yl)-amine 
• 61733-81-1 3,5,5-trimethyl-6-phenyl-4-oxa-1,2,6-triaza-5λ⁵-phospha-bicyclo[3.2.0]hept-2-en-7-one 

Relevant articles and documents

Stabilization of Azapeptides by Namide···H-NamideHydrogen Bonds

An unusual Namide···H-Namide hydrogen bond (HB) was previously proposed to stabilize the azapeptide β-Turns. Herein we provide experimental evidence for the Namide···H-Namide HB and show that this HB endows a stabilization of 1-3 kcal·mol-1 and enforces the trans-cis-Trans (t-c-T) and cis-cis-Trans (c-c-T) amide bond conformations in azapeptides and N-methyl-Azapeptides, respectively. Our results indicate that these Namide···H-Namide HBs can have stabilizing contributions even in short azapeptides that cannot fold to form β-Turns.

Superior reactivity of thiosemicarbazides in the synthesis of 2-amino-1,3,4-oxadiazoles

(Chemical Equation Presented) A facile and general protocol for the preparation of 2-amino-1,3,4-oxadiazoles is reported. This method relies on a tosyl chloride/pyridine-mediated cyclization of a thiosemicarbazide, which is readily prepared by acylation o

An efficient synthesis of 1,3,4-oxadiazoles from N,N′-diacylhydrazines using Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts as condensing agents

1,3,4-Oxadiazoles including 2-amino derivatives were effectively synthesized by treatment of N,N′-diacylhydrazines or N-acylsemicarbazides with Ph3P·Br2, Ph3P·CCl4 or Ph3P·CBr4 adducts in the presence of Et3N in CH2Cl2 under mild conditions.