141120-47-0

Basic information

• Product Name: 2-aza-3-phenyl-1-(3-pyridyl)prop-1-ene
• Synonyms: 2-aza-3-phenyl-1-(3-pyridyl)prop-1-ene
• CAS NO: 141120-47-0
• Molecular Weight: 196.252
• Mol File: 141120-47-0.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: 2-aza-3-phenyl-1-(3-pyridyl)prop-1-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-aza-3-phenyl-1-(3-pyridyl)prop-1-ene(141120-47-0)
• EPA Substance Registry System: 2-aza-3-phenyl-1-(3-pyridyl)prop-1-ene(141120-47-0)

Safety Data

• Hazardous Substances Data: 141120-47-0(Hazardous Substances Data)

Upstream product

• 500-22-1 3-pyridinecarboxaldehyde 
• 100-46-9 benzylamine 
• 100-47-0 benzonitrile 
• 3099-31-8 nicotinyl chloride 
• 622-79-7 benzyl azide 
• 100-55-0 3-hydroxymethylpyridin 

Downstream Products

• 63361-56-8 1-phenyl-N-(pyridin-3-ylmethyl)methanamine 
• 42977-21-9 1,2-bis(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)disulfide 
• 271583-67-6 2-(benzylamino)-2-(pyridin-3-yl)acetonitrile 
• 183016-48-0 diethyl (benzylamino)(pyridin-3-yl)methylphosphonate 
• 494-52-0 Anabasine 
• 31944-77-1 (2S)-N-benzyl-2-(3-pyridyl)-piperidine 
• 141120-60-7 (2S)-N-benzyl-2-(3-pyridyl)-4-piperidinone 
• 40179-50-8 (2S)-N-4'-nitrobenzoyl-2-(3-pyridyl)-4-piperidine 

Relevant articles and documents

Efficient Co-Catalyzed Double Hydroboration of Nitriles: Application to One-Pot Conversion of Nitriles to Aldimines

The commercially available and bench-stable Co(acac)2/dpephos system is employed as a precatalyst for selective and efficient room temperature hydroboration of organic nitriles with HBPin to produce a series of N,N-diborylamines [RN(BPin)2], which react in situ with aldehydes to give aldimines. Formation of aldimines from N,N-diborylamines does not require a dehydrating agent, is applicable to a wide range of N,N-diborylamine and aldehyde substrates and is highly chemoselective, being unaffected by various common functional groups, such as alkenes, alkynes, secondary amines, ketones, esters, amides, carboxylic acids, pyridines, nitriles, and nitro compounds. The overall transformation represents a synthetically valuable approach to aldimines from nitriles and can be performed in a sequential one-pot manner, tolerating ester, lactone, carboxamide and unactivated alkene functionalities.

Selective aerobic oxidation of halides and amines with an inorganic-ligand supported zinc catalyst

A practical, efficient and environmentally benign catalytic protocol for the oxidative cross-coupling reaction of halides with amines, oxidative self-coupling of amines and oxidation of halides was developed with inorganic-ligand supported ZnPOM (NH4)4[ZnMo6O18(OH)6] using molecular oxygen. This method mainly utilizes an inorganic polymolybdate ligand to support the Zn2+ ion, avoiding the use of complicated organic ligands.

Method for synthesizing imine through cross-coupling of hydroxylation phenanthroline copper complex/O2 catalytic oxidation alcohol and amine

The invention discloses a method for synthesizing imine through cross-coupling of hydroxylation phenanthroline copper complex/O2 catalytic oxidation alcohol and amine. According to the method, an economical and cheap hydroxylation phenanthroline copper complex is selected as a catalyst, green O2 is selected as an oxidizing agent, cross-coupling of alcohol and amine is realized under the condition of normal temperature, alkali and an expensive free radical of nitroxide is prevented from being used, and a series of imine compounds are successfully prepared. The method provided by the invention is high in reaction selectivity and relatively wide in a substrate application range, and has a great industrial application potential.