Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C3H8OS |
| Molecular Weight | 92.16 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[S+](C)[O-]
InChI
InChIKey=VTRRCXRVEQTTOE-UHFFFAOYSA-N
InChI=1S/C3H8OS/c1-3-5(2)4/h3H2,1-2H3
| Molecular Formula | C3H8OS |
| Molecular Weight | 92.16 |
| 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 |
|---|---|---|
| Intramolecular nonbonded S...N interaction in rabeprazole. | 2008-06 |
|
| Determination of the sulphoxides and sulphones of three simple sulphides in rat urine: effects of phenobarbitone, beta-naphthoflavone and methimazole. | 2005-01 |
|
| High sensitivity 1H-NMR spectroscopy of homeopathic remedies made in water. | 2004-11-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:29:46 GMT 2025
by
admin
on
Mon Mar 31 23:29:46 GMT 2025
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| Record UNII |
AAJ84LR4D8
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| Record Status |
Validated (UNII)
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| Record Version |
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AAJ84LR4D8
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1669-98-3
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121148
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admin on Mon Mar 31 23:29:46 GMT 2025 , Edited by admin on Mon Mar 31 23:29:46 GMT 2025
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