Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H10O2S |
| Molecular Weight | 170.229 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(C=C1)S(C)(=O)=O
InChI
InChIKey=YYDNBUBMBZRNQQ-UHFFFAOYSA-N
InChI=1S/C8H10O2S/c1-7-3-5-8(6-4-7)11(2,9)10/h3-6H,1-2H3
| Molecular Formula | C8H10O2S |
| Molecular Weight | 170.229 |
| 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 |
|---|---|---|
| 1-Benzyl-6,8-dimethyl-4-phenyl-2-tosyl-1,2,3,3a,4,6,7,8,9,9b-deca-hydro-pyrrolo[3,4-c]pyrano[6,5-d]pyrimidine-7,9-dione. | 2009-10-28 |
|
| Reduction of disulfide bonds within anti-D results in enhanced Fcgamma receptor blockade. | 2009-05 |
|
| Enantioselective synthesis of natural polyoxygenated cyclohexanes and cyclohexenes from [(p-tolylsulfinyl)methyl]-p-quinols. | 2007 |
|
| Study of regioselective methanesulfonylation of simple aromatics with methanesulfonic anhydride in the presence of zeolite catalysts. | 2004-11-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:58:02 GMT 2025
by
admin
on
Mon Mar 31 21:58:02 GMT 2025
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| Record UNII |
TG77SM513A
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| Record Status |
Validated (UNII)
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| Record Version |
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EPA PESTICIDE CODE |
601003
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