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 |
|---|---|---|
| FTIR monitoring of oxazolidin-5-one formation and decomposition in a glycolaldehyde-phenylalanine model system by isotope labeling techniques. | 2009-01-26 |
|
| Further insight into thermally and pH-induced generation of acrylamide from glucose/asparagine model systems. | 2008-08-13 |
|
| Tertiary aromatic amide for memory of chirality: access to enantioenriched alpha-substituted valine. | 2008-05-07 |
|
| Post-schiff base chemistry of the Maillard reaction: mechanism of imine isomerization. | 2008-04 |
|
| (4S)-Benzyl 4-isopropyl-5-oxo-1,3-oxazolidine-3-carboxyl-ate. | 2008-03-12 |
|
| Acrylamide formation in food: a mechanistic perspective. | 2005-03-12 |
|
| Why asparagine needs carbohydrates to generate acrylamide. | 2003-03-12 |
|
| A novel synthesis of N-methyl asparagine, arginine, histidine, and tryptophan. | 2002-10-17 |
|
| An unusual decarboxylative Maillard reaction between L-DOPA and D-glucose under biomimetic conditions: factors governing competition with Pictet-Spengler condensation. | 2001-07-27 |
|
| Enantioselective hydrolysis of potent amino acid precursors 5-oxazolidinone derivatives. | 2001 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:05:49 GMT 2025
by
admin
on
Mon Mar 31 23:05:49 GMT 2025
|
| Record UNII |
NSU4E5OEIG
|
| Record Status |
Validated (UNII)
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| Record Version |
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NSU4E5OEIG
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20510163
Created by
admin on Mon Mar 31 23:05:49 GMT 2025 , Edited by admin on Mon Mar 31 23:05:49 GMT 2025
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