17480-71-6

Basic information

• Product Name: (-)-Benzal-α-phenyl-ethylamin
• CAS NO: 17480-71-6
• Molecular Weight: 209.291
• Mol File: 17480-71-6.mol
• Article Data: 75

Chemical Properties

• CAS DataBase Reference: (-)-Benzal-α-phenyl-ethylamin(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-Benzal-α-phenyl-ethylamin(17480-71-6)
• EPA Substance Registry System: (-)-Benzal-α-phenyl-ethylamin(17480-71-6)

Safety Data

• Hazardous Substances Data: 17480-71-6(Hazardous Substances Data)

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 100-52-7 benzaldehyde 
• 3193-62-2 N-benzyl-1-phenylethylamine 
• 618-36-0 rac-methylbenzylamine 
• 3886-69-9 (+)-1-phenylethylamine 
• 128593-66-8 (R)-N-benzyl-(α-methyl-benzyl)amine hydrochloride 
• 38235-77-7 (R)-N-benzyl-1-phenylethylamine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 100-51-6 benzyl alcohol 
• 100-46-9 benzylamine 
• 591-51-5 phenyllithium 
• 100-47-0 benzonitrile 
• 32366-25-9 1-azidoethylbenzene 
• 2835-06-5 phenylglycin 

Downstream Products

• 78075-71-5 (4R,αS)-N(1)-(α-methylbenzyl)-4-phenylazetidin-2-one 
• 78075-70-4 N-[(S)-α-methylbenzyl]-4(S)-phenylazetidin-2-one 
• 89617-49-2 N-((S)-α-Phenylethyl)-3(S)-methyl-4(R)-trans-phenylazetidin-2-one 
• 89617-51-6 N-((S)-α-Phenylethyl)-3(R)-methyl-4(R)-cis-phenylazetidin-2-one 
• 89617-50-5 N-((S)-α-Phenylethyl)-3(S)-methyl-4(S)-cis-phenylazetidin-2-one 
• 89578-33-6 N-((S)-α-Phenylethyl)-3(R)-methyl-4(S)-trans-phenylazetidin-2-one 
• 135738-65-7 [Phenyl-((S)-1-phenyl-ethylamino)-methyl]-phosphonic acid dimethyl ester 
• 17480-69-2 (S)-N-benzyl-1-phenylethylamine 
• 168416-31-7 methyl 2-hydroxy-2-methyl-3-phenyl-3-(1-phenylethylamino)propanoate 
• 168610-03-5 methyl 2-hydroxy-2-methyl-3-phenyl-3-(1-phenylethylamino)propanoate 
• 10040-80-9 phenyl{[1-phenylethyl]amino}acetonitrile 
• 372951-50-3 [(R)-(Diphenyl-phosphinoyl)-phenyl-methyl]-((S)-1-phenyl-ethyl)-amine 

Relevant articles and documents

Co-catalytic oxidative coupling of primary amines to imines using an organic nanotube-gold nanohybrid

A novel nanohybrid structure was synthesized by assembling gold nanoparticles on polymerized polydiacetylene nanotubes. Combination of the nanohybrid with gallacetophenone afforded an efficient cooperative co-catalytic system for the oxidative coupling of primary amines into imines. The system is highly efficient and sustainable as it operates in high yields using minimal amounts of the metal and the quinone, under ambient atmosphere, at room temperature, in water, and is easily recycled.

Vanadium-and chromium-catalyzed dehydrogenative synthesis of imines from alcohols and amines

Vanadium(IV) tetraphenylporphyrin dichloride and chromium(III) tetraphenylporphyrin chloride have been developed as catalysts for the acceptorless dehydrogenation of alcohols. The catalysts have been applied to the direct synthesis of imines in overall good yields from a variety of alcohols and amines. The transformations are proposed to proceed by metal?ligand bifunctional pathways with an outer-sphere transfer of two hydrogen atoms from the alcohol to the metal porphyrin complexes. The results show that vanadium and chromium catalysts can also be employed for the dehydrogenation of alcohols with the release of hydrogen gas, and they may represent valuable alternatives to other catalysts based on Earth-abundant metals.

Manganese-Catalyzed Selective Hydrogenative Cross-Coupling of Nitriles and Amines to Form Secondary Imines

Manganese complexes with tridentate PNN ligands have been synthesized as catalysts for hydrogenative cross-coupling reaction of nitriles and amines to form secondary imines. This reaction afforded a variety of unsymmetrical secondary imines in good yields with excellent selectivity. Investigation of catalyst intermediates indicated that an amido manganese complex may be the active catalyst species for this reaction. (Figure presented.).