171513-98-7

Basic information

• Product Name: methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate
• Synonyms: methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate
• CAS NO: 171513-98-7
• Molecular Weight: 293.276
• Mol File: 171513-98-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate(171513-98-7)
• EPA Substance Registry System: methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate(171513-98-7)

Safety Data

• Hazardous Substances Data: 171513-98-7(Hazardous Substances Data)

Upstream product

• 160002-53-9 methyl (3R,4R,4'S)-(-)-3-N-benzyloxycarbonylamino-4-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-1-pyrazoline-3-carboxylate 
• 160002-54-0 methyl (1S,2R,4'S)-(-)-1-N-benzyloxycarbonylamino-2-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)cyclopropanecarboxylate 
• 160002-56-2 methyl (1S,2R,4'S)-(-)-1-N-benzyloxycarbonylamino-2-(1',3'-dioxolan-2'-thiocarbonyl-4'-yl)cyclopropanecarboxylate 
• 160002-57-3 (+)-N-benzyloxycarbonyl-γ,δ-dehydro-allo-coronamic acid methyl ester 
• 132970-32-2 methyl (4S,2Z)-2-benzyloxycarbonylamino-4,5-isopropylidenedioxy-2-pentanoate 
• 100945-15-1 N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester 
• 175694-63-0 methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-formylcyclopropanecarboxylate 
• 160002-55-1 methyl (1S,2R,1'S)-(-)-1-N-benzyloxycarbonylamino-2-(1',2'-dihydroxyethyl)cyclopropanecarboxylate 

Downstream Products

• 185527-68-8 (1S,2R)-1-Benzyloxycarbonylamino-2-chlorocarbonyl-cyclopropanecarboxylic acid methyl ester 
• 185527-69-9 (1S,2S)-1-Benzyloxycarbonylamino-2-methoxycarbonylmethyl-cyclopropanecarboxylic acid methyl ester 
• 185527-67-7 (-)-(Z)-2,3-methano-L-glutamic acid 

Relevant articles and documents

Enantioselective Total Syntheses of (-)-allo-Coronamic Acid, (-)-(Z)-2,3-Methanohomoserine, and (2S,3R)-Cbz-cyclo-Asp-OMe

The title amino acids have been synthesized in 45, 47, and 63percent overall yields, respectively, from enantiopure aminopentenoates, easily available from D-glyceraldehyde as a source of chirality, following divergent pathways from similar diols as commo