Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H5NO2 |
| Molecular Weight | 87.0773 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1CNCO1
InChI
InChIKey=GCSBYWTVHSKTNC-UHFFFAOYSA-N
InChI=1S/C3H5NO2/c5-3-1-4-2-6-3/h4H,1-2H2
| Molecular Formula | C3H5NO2 |
| Molecular Weight | 87.0773 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| An unusual decarboxylative Maillard reaction between L-DOPA and D-glucose under biomimetic conditions: factors governing competition with Pictet-Spengler condensation. | 2001 Jul 27 |
|
| Further insight into thermally and pH-induced generation of acrylamide from glucose/asparagine model systems. | 2008 Aug 13 |
|
| (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxyl-ate. | 2008 Mar 12 |
|
| FTIR monitoring of oxazolidin-5-one formation and decomposition in a glycolaldehyde-phenylalanine model system by isotope labeling techniques. | 2009 Jan 26 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:10:40 GMT 2023
by
admin
on
Sat Dec 16 10:10:40 GMT 2023
|
| Record UNII |
NSU4E5OEIG
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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6542-32-1
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NSU4E5OEIG
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admin on Sat Dec 16 10:10:40 GMT 2023 , Edited by admin on Sat Dec 16 10:10:40 GMT 2023
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20510163
Created by
admin on Sat Dec 16 10:10:40 GMT 2023 , Edited by admin on Sat Dec 16 10:10:40 GMT 2023
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