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 |
|---|---|---|
| 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. | 2008-01-23 |
|
| 3-Pyrrolidinecarboxylic acid for direct catalytic asymmetric anti-Mannich-type reactions of unmodified ketones. | 2006-08-02 |
|
| An efficient route to either enantiomer of orthogonally protected trans-3-aminopyrrolidine-4-carboxylic acid. | 2001-05-18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:17:53 GMT 2025
by
admin
on
Mon Mar 31 22:17:53 GMT 2025
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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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