Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H8OS |
| Molecular Weight | 140.203 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CSC1=CC=CC=C1O
InChI
InChIKey=SOOARYARZPXNAL-UHFFFAOYSA-N
InChI=1S/C7H8OS/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3
| Molecular Formula | C7H8OS |
| Molecular Weight | 140.203 |
| 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 |
|---|---|---|
| Gain of a 500-fold sensitivity on an intravital MR contrast agent based on an endohedral gadolinium-cluster-fullerene-conjugate: a new chance in cancer diagnostics. | 2010-05-28 |
|
| Towards [Cp*Rh(bpy)(H2O]2+-promoted P450 catalysis: direct regeneration of CytC. | 2009-03 |
|
| Treatment of glioblastoma multiforme cells with temozolomide-BioShuttle ligated by the inverse Diels-Alder ligation chemistry. | 2009-02-06 |
|
| S,C-sulfonium ylides from thiophenes: potential carbene precursors. | 2007-12-26 |
|
| Alpha,omega-bis(thioacetyl)oligophenylenevinylene chromophores from thioanisol precursors. | 2004-02-20 |
|
| New aspects of the reactivity of tyrosinase. | 2004 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:13:54 GMT 2025
by
admin
on
Mon Mar 31 19:13:54 GMT 2025
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| Record UNII |
A6JO803536
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| Record Status |
Validated (UNII)
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| Record Version |
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JECFA EVALUATION |
O-(METHYLTHIO)PHENOL
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