1403953-55-8

Basic information

• Product Name: (1S,2S)-benzyl 2-(diphenylmethylideneamino)cyclopropanecarboxylate
• Synonyms: (1S,2S)-benzyl 2-(diphenylmethylideneamino)cyclopropanecarboxylate
• CAS NO: 1403953-55-8
• Molecular Weight: 355.436
• Mol File: 1403953-55-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S)-benzyl 2-(diphenylmethylideneamino)cyclopropanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-benzyl 2-(diphenylmethylideneamino)cyclopropanecarboxylate(1403953-55-8)
• EPA Substance Registry System: (1S,2S)-benzyl 2-(diphenylmethylideneamino)cyclopropanecarboxylate(1403953-55-8)

Safety Data

• Hazardous Substances Data: 1403953-55-8(Hazardous Substances Data)

Upstream product

• 182748-72-7 (R)-3-((tert-butoxycarbonyl)amino)-4-hydroxybutyric acid benzyl ester 
• 51186-58-4 4-benzyl Boc-D-aspartate 
• 1403953-52-5 (3R)-benzyl 3-(diphenylmethylideneamino)-4-iodobutanoate 
• 1418006-26-4 (3R)-benzyl 3-amino-4-iodobutanoate hydrochloride 

Downstream Products

• 1403953-57-0 (1S,2S)-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid 
• 1403953-59-2 (1'S,2'S)-methyl [(2'-diphenylmethylideneaminocyclopropane)carbonyl]aminoacetate 

Relevant articles and documents

Stereoselective synthesis of both enantiomers of trans-2- (diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides

The stereoselective synthesis of (1R,2R)- and (1S,2S)-trans-2- (diphenylmethylideneamino)cyclopropanecarboxylic acid has been accomplished in six steps starting from (2S)- and (2R)-β-benzyl N-(tert-butoxycarbonyl) aspartate, respectively. The key-step in