1285695-88-6

Basic information

• Product Name: (S)-N-(bis(3,5-dimethylphenyl)methylene)-1-(3-bromophenyl)but-3-en-1-amine
• Synonyms: (S)-N-(bis(3,5-dimethylphenyl)methylene)-1-(3-bromophenyl)but-3-en-1-amine
• CAS NO: 1285695-88-6
• Molecular Weight: 446.43
• Mol File: 1285695-88-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N-(bis(3,5-dimethylphenyl)methylene)-1-(3-bromophenyl)but-3-en-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(bis(3,5-dimethylphenyl)methylene)-1-(3-bromophenyl)but-3-en-1-amine(1285695-88-6)
• EPA Substance Registry System: (S)-N-(bis(3,5-dimethylphenyl)methylene)-1-(3-bromophenyl)but-3-en-1-amine(1285695-88-6)

Safety Data

• Hazardous Substances Data: 1285695-88-6(Hazardous Substances Data)

Upstream product

• 22679-40-9 3,3’,5,5’-tetramethylbenzophenone 
• 21945-78-8 bis(3,5-dimethylphenyl)methanol 
• 22445-42-7 3,5-dimethylbenzonitrile 
• 556-96-7 5-bromo-1,3-xylene 
• 3132-99-8 m-bromobenzoic aldehyde 
• 1285695-66-0 1,1-bis(3,5-dimethylphenyl)but-3-en-1-amine 
• 1285695-94-4 (R)-N-(bis(3,5-dimethylphenyl)methylene)hept-1-en-4-amine 

Downstream Products

• 1285696-18-5 (S)-1-(3-bromophenyl)but-3-en-1-amine hydrochloride 

Relevant articles and documents

Direct catalytic asymmetric aminoallylation of aldehydes: Synergism of chiral and nonchiral Bronsted acids

The development of a catalytic asymmetric method for the direct aminoallylation of aldehydes is described that gives high asymmetric inductions for a broad range of substrates including both aromatic and aliphatic aldehydes. This method allows for direct isolation of unprotected analytically pure homoallylic amines without chromatography. The unique catalyst system developed for this process involves the synergistic interaction between a chiral and a nonchiral Bronsted acid.