Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H16O4S |
| Molecular Weight | 232.297 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)[C@@H]2CC[C@@]1(CS(O)(=O)=O)C(=O)C2
InChI
InChIKey=MIOPJNTWMNEORI-GMSGAONNSA-N
InChI=1S/C10H16O4S/c1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h7H,3-6H2,1-2H3,(H,12,13,14)/t7-,10-/m1/s1
| Molecular Formula | C10H16O4S |
| Molecular Weight | 232.297 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:18:09 GMT 2025
by
admin
on
Mon Mar 31 18:18:09 GMT 2025
|
| Record UNII |
9TLZ01S15L
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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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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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C851
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C77132
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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m3006
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | Merck Index | ||
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221-554-1
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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3144-16-9
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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CAMPHORSULFONIC ACID
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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DTXSID00883956
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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1087520
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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9TLZ01S15L
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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100000144027
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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SUB127698
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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55379
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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SUB191204
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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ALTERNATIVE | |||
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SUB120778
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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55403
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY | |||
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65617
Created by
admin on Mon Mar 31 18:18:09 GMT 2025 , Edited by admin on Mon Mar 31 18:18:09 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
RACEMATE -> ENANTIOMER |
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ENANTIOMER -> ENANTIOMER |
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT |