1883-96-1

Basic information

• Product Name: N-[(E)-phenylmethylidene]pyridin-2-amine
• Synonyms: 2-Pyridinamine, N-(phenylmethylene)-; 2-pyridinamine, N-[(1E)-phenylmethylene]-; N-(Phenylmethylene)-2-pyridinamine; N-[(E)-Phenylmethylene]pyridin-2-amine
• CAS NO: 1883-96-1
• Molecular Formula: C₁₂H₁₀N₂
• Molecular Weight: 182.2212
• Mol File: 1883-96-1.mol
• Article Data: 50

Chemical Properties

• Boiling Point: 324.162°C at 760 mmHg
• Flash Point: 149.848°C
• Density: 1.023g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.575
• CAS DataBase Reference: N-[(E)-phenylmethylidene]pyridin-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(E)-phenylmethylidene]pyridin-2-amine(1883-96-1)
• EPA Substance Registry System: N-[(E)-phenylmethylidene]pyridin-2-amine(1883-96-1)

Safety Data

• Hazardous Substances Data: 1883-96-1(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 100-52-7 benzaldehyde 
• 41855-95-2 N,N¹--α,α-diaminotoluene 
• 71-43-2 benzene 
• 27200-79-9 p-bromophenylacetaldehyde 
• 538-51-2 benzylidene phenylamine 
• 100-51-6 benzyl alcohol 
• 23574-81-4 N-(triphenylphosphoranylidene)pyridin-2-amine 
• 108-88-3 toluene 
• 108-93-0 cyclohexanol 

Downstream Products

• 64138-49-4 N-(1-phenylethyl)pyridin-2-ylamine 
• 93725-14-5 N,N-dimethyl-N'-(1-phenyl-ethyl)-N'-[2]pyridyl-ethylenediamine 
• 96354-74-4 N-(diphenylmethyl)pyridin-2-amine 
• 74037-48-2 N-(1,2-diphenylethyl)pyridin-2-amine 
• 63232-84-8 N-(morpholin-4-yl-phenyl-methyl)-N-pyridin-2-yl-benzamide 
• 10254-52-1 2-phenyl-3-(pyridin-2-yl)-1,3-thiazolidin-4-one 
• 54214-70-9 2,3-diphenyl-4H-pyrido[1,2-a]pyrimidin-4-one 
• 59046-00-3 3-chloro-2-phenylpyrido<1,2-a>pyrimidin-4(4H)-one 
• 91538-37-3 3,3-dichloro-4-phenyl-1-(2-pyridyl)-2-azetidinone 
• 91538-38-4 methyl 2,2-dichloro-3-phenyl-3-(2-pyridylamino)propanoate 
• 159639-04-0 4,4-dimethyl-1-phenyl-1-(pyridin-2-yl)aminopropan-3-one 
• 91538-35-1 2,2-dichloro-3-phenyl-3-(2-pyridylamino)propanoic acid 
• 64413-91-8 2-phenyl-3-chloroimidazo<1,2-a>pyridine 
• 4044-95-5 2-Phenyl-3-bromoimidazo<1,2-a>pyridine 

Relevant articles and documents

Study of N-benzylidene derivatives synthesized as corrosion inhibitors for copper in HCl solution

Corrosion inhibition of the two N-benzylidene derivative compounds, namely N-benzylidene pyridin-2 amine (NBPA) and N-(4-choloromethylbenzylidene) pyridin-2 amine (NCMBPA) as corrosion inhibitors for copper in hydrochloric acid 6.0 M have been studied by

Functional POM-catalyst for selective oxidative dehydrogenative couplings under aerobic conditions

Development of selective and efficient reusable catalytic systems for sustainable chemical production under benign conditions is attractive and received much attention. Herein, we report a rod-shaped octadecyl trimethylammonium functionalized Keggin-type polyoxometalate [PMO12O40] hybrids (OTA-POM) as an efficient heterogeneous catalyst for selective oxidative dehydrogenative couplings under aerobic conditions without any additive or external base. The catalyst recovery and subsequent five successive recyclability studies of hybrid POM confirms the heterogeneous nature of present catalytic system.

Rh(III)-Catalyzed imidoyl C-H carbamylation and cyclization to bicyclic [1,3,5]triazinones

A Rh(III)-catalyzed synthesis of bicyclic [1,3,5]-triazinones from a diverse array of imines coupled with ethyl (pivaloyloxy)carbamate is reported. The preparation of [5,6]- and [6,6]-bicyclic heterocycles substituted with aryl, alkyl, and alkoxy groups demonstrated a broad reaction scope. The efficiency of this approach was further enhanced with the development of a three-component variant featuring in situ imine formation. X-ray crystallographic characterization of a rhodacycle formed by imidoyl C-H activation provides support for the proposed mechanism.