Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H10O4 |
| Molecular Weight | 134.1305 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1OC[C@H](O)[C@H]1O
InChI
InChIKey=KZVAAIRBJJYZOW-VPENINKCSA-N
InChI=1S/C5H10O4/c6-1-4-5(8)3(7)2-9-4/h3-8H,1-2H2/t3-,4+,5+/m0/s1
| Molecular Formula | C5H10O4 |
| Molecular Weight | 134.1305 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:58:43 GMT 2023
by
admin
on
Sat Dec 16 19:58:43 GMT 2023
|
| Record UNII |
8XWR7NN42F
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
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Official Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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100000172586
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | |||
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258-560-9
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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8XWR7NN42F
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | |||
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1307762
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | RxNorm | ||
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104501
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | |||
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53448-53-6
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | |||
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8XWR7NN42F
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
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PRIMARY | |||
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C096716
Created by
admin on Sat Dec 16 19:58:43 GMT 2023 , Edited by admin on Sat Dec 16 19:58:43 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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RACEMATE -> ENANTIOMER |
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