4916-20-5

Basic information

• Product Name: 3-anilinopropanehydrazide
• CAS NO: 4916-20-5
• Molecular Formula: C₉H₁₃N₃O
• Molecular Weight: 179.219
• Mol File: 4916-20-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 443.3°C at 760 mmHg
• Flash Point: 221.9°C
• Density: 1.182g/cm³
• Vapor Pressure: 4.69E-08mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: 3-anilinopropanehydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-anilinopropanehydrazide(4916-20-5)
• EPA Substance Registry System: 3-anilinopropanehydrazide(4916-20-5)

Safety Data

• Hazardous Substances Data: 4916-20-5(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 5652-38-0 N-phenyl-β-alanine 
• 21911-84-2 methyl 3-(phenylamino)propanoate 

Downstream Products

• 1135453-49-4 3-(phenylamino)-N-[(phenylcarbamoyl)amino]propanamide 
• 1135453-53-0 3-[phenyl(phenylcarbamoyl)amino]-N-[(phenylcarbamoyl)amino]propanamide 
• 1135453-55-2 3-[phenyl(phenylthiocarbamoyl)amino]-N-[(phenylthiocarbamoyl)amino]propanamide 
• 1135453-47-2 N-(2,5-dimethyl-1H-pyrrol-1-yl)-3-(phenylamino)propanamide 
• 1135453-46-1 1-(3,5-dimethyl-1H-pyrazol-1-yl)-3-(phenylamino)propan-1-one 
• 1664-40-0 N-(2-aminoethyl)benzeneamine 
• 864186-60-7 4-phenyl-5-[2-(phenylamino)ethyl]-2,4-dihydro-3H-1,2,4-triazole-3-thione 

Relevant articles and documents

Synthesis and characterization of N-substitutional ethylenediamine derivatives

N-Substituted and N,N-disubstituted ethylenediamine derivatives were prepared rapidly in aqueous conditions from 30 to 76 % yields, respectively, on a multi-gram scale starting from inexpensive and commercially available starting materials. The steps involved Michael addition, hydrazinolysis and Curtius rearrangements. The highlight of this method lies on its convenience and economy in accessing these intermediates.

Synthesis of azole derivatives from 3-phenylaminopropanohydrazide and evaluation of their antimicrobial efficacy

Novel pyrrole and pyrazole derivatives containing phenylaminopropanoyl moiety were synthesized from 3-phenylaminopropanohydrazide through its condensation with diketones. The intramolecular cyclization reaction of disubstituted semicarbazides and thiosemi