88328-13-6

Basic information

• Product Name: 1-phenyl-N-(2-(pyridin-2-yl)methyl)methanimine
• Synonyms: 1-phenyl-N-(2-(pyridin-2-yl)methyl)methanimine
• CAS NO: 88328-13-6
• Molecular Weight: 196.252
• Mol File: 88328-13-6.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 1-phenyl-N-(2-(pyridin-2-yl)methyl)methanimine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-N-(2-(pyridin-2-yl)methyl)methanimine(88328-13-6)
• EPA Substance Registry System: 1-phenyl-N-(2-(pyridin-2-yl)methyl)methanimine(88328-13-6)

Safety Data

• Hazardous Substances Data: 88328-13-6(Hazardous Substances Data)

Upstream product

• 3731-51-9 2-(Aminomethyl)pyridine 
• 100-52-7 benzaldehyde 
• 19198-87-9 N-[(1E)-pyridin-2-ylmethylidene]benzenemethanamine 
• 100-46-9 benzylamine 
• 622-79-7 benzyl azide 
• 10029-90-0 trans-2-phenyl-3-(2-pyridyl)aziridine 
• 504-29-0 2-aminopyridine 
• 100-51-6 benzyl alcohol 
• 129760-63-0 C₉H₁₄NSi^(1-)*Li⁽¹⁺⁾ 
• 17881-80-0 (2-picolyl)trimethylsilane 

Downstream Products

• 90-02-8 salicylaldehyde 
• 137129-33-0 2-((pyridin-2-ylmethylimino)methyl)phenol 
• 1256973-99-5 (2S,3R,4S,5R)-4-benzoyl-2,3-diphenyl-5-(2-pyridyl)pyrrolidine 
• 1256973-97-3 (2S,3R,4S,5R)-4-nitro-2,3-diphenyl-5-(2-pyridyl)pyrrolidine 
• 1256974-04-5 4-nitro-2,3-diphenyl-5-(2-pyridyl)pyrrolidine 
• 1256973-93-9 (3aS,4S,6R,6aR)-4-(2-fluorophenyl)-2-methyl-6-(2-pyridyl)octahydropyrrolo[3,4-c]pyrrole-1,3-dione 
• 1256974-00-1 4-(2-fluorophenyl)-2-methyl-6-(2-pyridyl)octahydropyrrolo[3,4-c]pyrrole-1,3-dione 
• 1256973-70-2 (3aS,4S,6R,6aR)-2-methyl-4-phenyl-6-(2-pyridyl)-octahydropyrrolo[3,4-c]pyrrole-1,3-dione 
• 18081-89-5 2-(N-benzylaminomethyl)pyridine 
• 663151-73-3 [(cyclopentadienyl)(.kappa2-N,N'-(N-(phenylmethylene)-2-picolylamine))(acetonitrile)ruthenium(II)] hexafluorophosphate 
• 105877-23-4 (PtCl₂(C₅H₄N)CH₂NCH(C₆H₅)) 
• 121020-53-9 2-(4-Methoxy-phenyl)-1-pyridin-2-yl-ethylamine 
• 139439-02-4 2-(4-Chloro-phenyl)-1-pyridin-2-yl-ethylamine 
• 139439-03-5 1-(pyridin-2-yl)but-3-en-1-amine 

Relevant articles and documents

Rh(i)-catalysed imine-directed C-H functionalization: via the oxidative [3 + 2] cycloaddition of benzylamine derivatives with maleimides

The Rh(i)-catalysed imine-directed oxidative [3 + 2] cycloaddition of benzylamines with maleimides is reported. A wide range of both benzylamines and maleimides is applicable to the reaction. A one-pot three component strategy using benzylamines, 2-pyridi

Aerobic C?H Hydroxylation by Copper Imine Complexes: The Clip-and-Cleave Concept – Versatility and Limits

The intramolecular ligand hydroxylation of a series of copper(I) imine complexes during their reaction with dioxygen had been systematically studied. The so-called clip-and-cleave concept offers a facile way to oxygenate aldehydes or ketones. A copper(I)

Direct and Stereospecific [3+2] Synthesis of Pyrrolidines from Simple Unactivated Alkenes

Pyrrolidines are important heterocyclic compounds with endless applications in organic synthesis, metal catalysis, and organocatalysis. Their potential as ligands for first-row transition-metal catalysts inspired a new method to access complex poly-heterocyclic pyrrolidines in one step from available materials. This fundamental step forward is based on the discovery of an essential organoaluminum promoter that engages unactivated and electron-rich olefins in intermolecular [3+2] cycloadditions.