869800-29-3

Basic information

• Product Name: benzyl (S)-[(2-chloro-ethyl)-(1-phenyl-ethyl)-amino]ethanoate
• CAS NO: 869800-29-3
• Molecular Weight: 331.842
• Mol File: 869800-29-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl (S)-[(2-chloro-ethyl)-(1-phenyl-ethyl)-amino]ethanoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (S)-[(2-chloro-ethyl)-(1-phenyl-ethyl)-amino]ethanoate(869800-29-3)
• EPA Substance Registry System: benzyl (S)-[(2-chloro-ethyl)-(1-phenyl-ethyl)-amino]ethanoate(869800-29-3)

Safety Data

• Hazardous Substances Data: 869800-29-3(Hazardous Substances Data)

Upstream product

• 6623-43-4 (S)-(-)-N-(2-hydroxyethyl)-α-methylbenzylamine 
• 869800-28-2 benzyl (S)-[(2-hydroxy-ethyl)-(1-phenyl-ethyl)-amino]ethanoate 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 249734-37-0 benzyl [1(1S,2R)]-1-(1-phenyl-ethyl)-azetidine-2-carboxylate 
• 247051-66-7 benzyl [1(1S,2S)]-1-(1-phenyl-ethyl)-azetidine-2-carboxylate 

Relevant articles and documents

Practical asymmetric preparation of azetidine-2-carboxylic acid

Facile and straightforward syntheses of both enantiomers of azetidine-2-carboxylic acid are described. The syntheses depart from inexpensive chemicals and allow for the production, in five to six steps, of practical quantities of each enantiomer. Synthetic highlights include the construction of the azetidine ring using an intramolecular alkylation and the use of optically active α-methylbenzylamine as chiral auxiliary.