Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C4H4O4 |
| Molecular Weight | 116.0722 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1OC(=O)OC1=O
InChI
InChIKey=JLXQJNCZXSYXAK-UHFFFAOYSA-N
InChI=1S/C4H4O4/c1-2-3(5)8-4(6)7-2/h2H,1H3
| Molecular Formula | C4H4O4 |
| Molecular Weight | 116.0722 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:40:42 GMT 2025
by
admin
on
Wed Apr 02 08:40:42 GMT 2025
|
| Record UNII |
G27CEX5CF8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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17578-13-1
Created by
admin on Wed Apr 02 08:40:42 GMT 2025 , Edited by admin on Wed Apr 02 08:40:42 GMT 2025
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PRIMARY | |||
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Lactic acid O-carboxyanhydride
Created by
admin on Wed Apr 02 08:40:42 GMT 2025 , Edited by admin on Wed Apr 02 08:40:42 GMT 2025
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PRIMARY | |||
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DTXSID401030440
Created by
admin on Wed Apr 02 08:40:42 GMT 2025 , Edited by admin on Wed Apr 02 08:40:42 GMT 2025
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PRIMARY | |||
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G27CEX5CF8
Created by
admin on Wed Apr 02 08:40:42 GMT 2025 , Edited by admin on Wed Apr 02 08:40:42 GMT 2025
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PRIMARY | |||
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22227598
Created by
admin on Wed Apr 02 08:40:42 GMT 2025 , Edited by admin on Wed Apr 02 08:40:42 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ENANTIOMER -> RACEMATE |
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ENANTIOMER -> RACEMATE |
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