765241-71-2

Basic information

• Product Name: Cyclopropaneacetic acid, 2-amino-2-carboxy-, (1R-cis)- (9CI)
• Synonyms: Cyclopropaneacetic acid, 2-amino-2-carboxy-, (1R-cis)- (9CI)
• CAS NO: 765241-71-2
• Molecular Formula: C6H9NO4
• Molecular Weight: 159.13996
• Product Categories: GLYCINESCAFFOLD;CARBOXYLICACID
• Mol File: 765241-71-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 416.2±20.0 °C(Predicted)
• Appearance: /
• Density: 1.534±0.06 g/cm3(Predicted)
• PKA: 2.70±0.50(Predicted)
• CAS DataBase Reference: Cyclopropaneacetic acid, 2-amino-2-carboxy-, (1R-cis)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropaneacetic acid, 2-amino-2-carboxy-, (1R-cis)- (9CI)(765241-71-2)
• EPA Substance Registry System: Cyclopropaneacetic acid, 2-amino-2-carboxy-, (1R-cis)- (9CI)(765241-71-2)

Safety Data

• Hazardous Substances Data: 765241-71-2(Hazardous Substances Data)

Upstream product

• 116447-37-1 dimethyl N-benzyloxycarbonyl-2,3-methanoglutamate 
• 116447-43-9 (Z)-2-Benzyloxycarbonylamino-pent-2-enedioic acid 
• 116447-36-0 methoxycarbonylmethyl-3-benzyloxycarbamide-3-carbomethoxy-Δ¹-pyrazoline 
• 145306-60-1 (+)-(2R,3R)-N-propionyl-2,3-methanopyroglutamic acid methyl ester 
• 104754-53-2 N-benzyloxycarbonyl-α-benzyl-(Z)-α,β-dehydroglutamate 
• 145241-91-4 γ-methyl N-benzyloxycarbonyl-(Z)-2,3-methanoglutamic acid α-benzyl ester 
• 145241-90-3 4-methoxycarbonylmethyl-3-benzyloxycarbonylamino-3-benzyloxycarbonyl-1-pyrazoline 
• 145631-97-6 (+)-(2R,3S)-2,3-methanoproline methyl ester 
• 116447-40-6 (+/-)-2,3-methanopyroglutamic acid 
• 145631-96-5 (+)-(2R,3S)-N-propionyl-2,3-methanopropline methyl ester 
• 145306-59-8 (+)-(2R,3S)-N-benzyloxycarbonyl-2,3-methanopropline methyl ester 
• 145241-95-8 (-)-(2S,3S)-N-propionyl-2,3-methanopyroglutamic acid methyl ester 
• 185527-69-9 (1S,2S)-1-Benzyloxycarbonylamino-2-methoxycarbonylmethyl-cyclopropanecarboxylic acid methyl ester 
• 171513-98-7 methyl (1S,2R)-(-)-1-N-benzyloxycarbonylamino-2-carboxycyclopropanecarboxylate 

Relevant articles and documents

First enantioselective synthesis of (-)-(Z)-2,3-methano-L-glutamic acid

(-)-(Z)-2,3-Methano-L-glutamic acid, a potential mGluR agonist, has been synthesized for the first time in 40% overall yield from a homochiral amino pentenoate as an easily available precursor. A conveniently protected (-)-(Z)-cyclo-aspartic acid derivati

Synthesis of 2,3-Methano-glutamic and -pyroglutamic Acid

2,3-Methano-analogues of glutamic and pyroglutamic acid have been synthesized and the β-naphthylamide of the latter is shown to be stable to pyroglutamic amino peptidase; the crystal structure of the methyl pyroglutamate analogue has been determined.