447415-96-5

Basic information

• Product Name: tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)propanoate
• Synonyms: tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)propanoate
• CAS NO: 447415-96-5
• Molecular Weight: 571.498
• Mol File: 447415-96-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)propanoate(447415-96-5)
• EPA Substance Registry System: tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)propanoate(447415-96-5)

Safety Data

• Hazardous Substances Data: 447415-96-5(Hazardous Substances Data)

Upstream product

• 120343-46-6 (S)-N-benzyl-N-(α-methyl-p-methoxybenzyl)amine 
• 403705-03-3 tert-butyl (E)-3-(2-iodophenyl)prop-2-enoate 
• 27784-76-5 tert-butyl diethylphosphonoacetate 
• 26260-02-6 2-iodobenzaldehyde 

Downstream Products

• 447416-17-3 tert-butyl (3R,αS)-3-(2-iodophenyl)-3-(N-α-methyl-4-methoxybenzylamino)propanoate 

Relevant articles and documents

Asymmetric synthesis of β-haloaryl β-amino acid derivatives

Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide may be employed as a homochiral ammonia equivalent for the synthesis of homochiral β-haloaryl β-amino acid derivatives via a strategy involving its conjugate addition to α,β-unsaturated β-haloaryl acceptors and subsequent oxidative deprotection with ceric ammonium nitrate.