Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H16N2O3S |
| Molecular Weight | 244.311 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNCC(O)C1=CC=CC(NS(C)(=O)=O)=C1
InChI
InChIKey=ZHOWHMXTJFZXRB-UHFFFAOYSA-N
InChI=1S/C10H16N2O3S/c1-11-7-10(13)8-4-3-5-9(6-8)12-16(2,14)15/h3-6,10-13H,7H2,1-2H3
| Molecular Formula | C10H16N2O3S |
| Molecular Weight | 244.311 |
| 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
Mon Mar 31 18:49:34 GMT 2025
by
admin
on
Mon Mar 31 18:49:34 GMT 2025
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| Record UNII |
7E2P22546V
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Code | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29709
Created by
admin on Mon Mar 31 18:49:34 GMT 2025 , Edited by admin on Mon Mar 31 18:49:34 GMT 2025
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| Code System | Code | Type | Description | ||
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DTXSID40862664
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SUB00442MIG
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CHEMBL146408
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C79522
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155
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AMIDEPHRINE
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C016980
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37571-84-9
Created by
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3354-67-4
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SUPERSEDED | |||
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100000085151
Created by
admin on Mon Mar 31 18:49:34 GMT 2025 , Edited by admin on Mon Mar 31 18:49:34 GMT 2025
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m1663
Created by
admin on Mon Mar 31 18:49:34 GMT 2025 , Edited by admin on Mon Mar 31 18:49:34 GMT 2025
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PRIMARY | Merck Index | ||
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7E2P22546V
Created by
admin on Mon Mar 31 18:49:34 GMT 2025 , Edited by admin on Mon Mar 31 18:49:34 GMT 2025
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15010
Created by
admin on Mon Mar 31 18:49:34 GMT 2025 , Edited by admin on Mon Mar 31 18:49:34 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |