Details
Stereochemistry | RACEMIC |
Molecular Formula | C5H9NO2 |
Molecular Weight | 115.1305 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1CCNC1
InChI
InChIKey=JAEIBKXSIXOLOL-UHFFFAOYSA-N
InChI=1S/C5H9NO2/c7-5(8)4-1-2-6-3-4/h4,6H,1-3H2,(H,7,8)
Molecular Formula | C5H9NO2 |
Molecular Weight | 115.1305 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
An efficient route to either enantiomer of orthogonally protected trans-3-aminopyrrolidine-4-carboxylic acid. | 2001 May 18 |
|
3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones. | 2006 Aug 2 |
|
Catalysis of 3-pyrrolidinecarboxylic acid and related pyrrolidine derivatives in enantioselective anti-Mannich-type reactions: importance of the 3-acid group on pyrrolidine for stereocontrol. | 2008 Jan 23 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:45:56 GMT 2023
by
admin
on
Sat Dec 16 08:45:56 GMT 2023
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Record UNII |
XQ9918NB1D
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Record Status |
Validated (UNII)
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Record Version |
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