Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H14S2 |
| Molecular Weight | 246.391 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C(SSCC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=GVPWHKZIJBODOX-UHFFFAOYSA-N
InChI=1S/C14H14S2/c1-3-7-13(8-4-1)11-15-16-12-14-9-5-2-6-10-14/h1-10H,11-12H2
| Molecular Formula | C14H14S2 |
| Molecular Weight | 246.391 |
| 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 |
|---|---|---|
| Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors. | 1996 Sep 13 |
|
| Fungal cleavage of thioether bond found in Yperite. | 1997 Jul 28 |
|
| Sulfur compounds reduce potato toxins during extrusion cooking. | 2001 Jun |
|
| Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenides. | 2003 Nov 5 |
|
| Patch testing with components of water-based metalworking fluids: results of a multicentre study with a second series. | 2006 Dec |
|
| A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry. | 2009 Nov 23 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:57:27 GMT 2023
by
admin
on
Fri Dec 15 18:57:27 GMT 2023
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| Record UNII |
BG7680605N
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| Record Status |
Validated (UNII)
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| Record Version |
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JECFA EVALUATION |
BENZYL DISULFIDE
Created by
admin on Fri Dec 15 18:57:27 GMT 2023 , Edited by admin on Fri Dec 15 18:57:27 GMT 2023
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CFR |
21 CFR 172.515
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150-60-7
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m4288
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C492349
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