Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8S |
| Molecular Weight | 136.214 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CSC1=CC=CC=C1
InChI
InChIKey=GMPDOIGGGXSAPL-UHFFFAOYSA-N
InChI=1S/C8H8S/c1-2-9-8-6-4-3-5-7-8/h2-7H,1H2
| Molecular Formula | C8H8S |
| Molecular Weight | 136.214 |
| 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 |
|---|---|---|
| Efficient synthesis and subsequent transformations of phenylsulfanylbicyclo[2.2.2]octenones and phenylselenylbicyclo[2.2.2]octenones. | 2009-02-20 |
|
| Tin-free generation of alkyl radicals from alkyl 4-pentynyl sulfides via homolytic substitution at the sulfur atom. | 2008-03-20 |
|
| Analogs of squalene and oxidosqualene inhibit oxidosqualene cyclase of Trypanosoma cruzi expressed in Saccharomyces cerevisiae. | 2005-12 |
|
| Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. | 2004-12-24 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:05:45 GMT 2025
by
admin
on
Mon Mar 31 19:05:45 GMT 2025
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| Record UNII |
253GML9Q62
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| Record Status |
Validated (UNII)
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| Record Version |
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217-351-2
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1822-73-7
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253GML9Q62
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