13820-19-4

Basic information

• Product Name: Propanedinitrile, [1-(phenylamino)ethylidene]-
• CAS NO: 13820-19-4
• Molecular Formula: C11H9N3
• Molecular Weight: 183.213
• Mol File: 13820-19-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Propanedinitrile, [1-(phenylamino)ethylidene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedinitrile, [1-(phenylamino)ethylidene]-(13820-19-4)
• EPA Substance Registry System: Propanedinitrile, [1-(phenylamino)ethylidene]-(13820-19-4)

Safety Data

• Hazardous Substances Data: 13820-19-4(Hazardous Substances Data)

Upstream product

• 93102-15-9 bis-(cyano) methylene-11 ethano-9,10 dihydro-9,10 anthracene 
• 62-53-3 aniline 
• 91255-14-0 α-Cyano-β-N-phenylaminocrotonamide 
• 68-12-2 N,N-dimethyl-formamide 
• 1445-45-0 Trimethyl orthoacetate 
• 109-77-3 malononitrile 
• 62321-92-0 α-cyano-β-dimethylaminocrotonamide 

Downstream Products

• 352554-06-4 4-amino-5-benzoyl-2-methyl-1-phenyl-1H-pyrrole-3-carbonitrile 
• 352555-25-0 3,4-diamino-2-benzoyl-6-dimethylamino-1-phenylpyrrolo[3,2-c]dipyrido[b,d]thiophene 
• 360062-36-8 3-amino-2-benzoyl-4-cyano-5-(3-cyano-4-dimethylamino-2-pyridyl)mercaptomethyl-1-phenylpyrrole 
• 360062-35-7 3-amino-2-benzoyl-5-bromomethyl-4-cyano-1-phenylpyrrole 
• 360062-33-5 3-amino-2-benzoyl-4-carbamoyl-5-methyl-1-phenylpyrrole 
• 360062-30-2 4-cyano-3-dimethylaminomethinamino-2-methoxycarbonyl-5-methyl-1-phenylpyrrole 
• 352554-07-5 3-amino-4-cyano-5-methyl-2-methoxycarbonyl-1-phenylpyrrole 

Relevant articles and documents

Torp-Ziegler cyclization in the synthesis of 3-amino-4-cyanopyrrole derivatives

Polyfunctional derivatives of 3-aminopyrrole have been synthesized from several substituted β-enamino nitriles using Torp-Ziegler cyclization. These compounds are starting materials for further conversions, particularly for the synthesis of pyrrolo[3,2-d]

β,β-Diacyl-enamine und -enole, 9. Zur Darstellung von Aminomethylenderivaten offenkettiger CH2-acider Verbindungen

The reaction of a combination of primary or secondary aromatic or aliphatic amines with orthocarboxylic esters upon a variety of open-chain CH2-acidic molecules gives N-substituted aminoalkylidene derivatives.The method is highly recommended for methylene