Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH4S2 |
| Molecular Weight | 80.172 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
SCS
InChI
InChIKey=INBDPOJZYZJUDA-UHFFFAOYSA-N
InChI=1S/CH4S2/c2-1-3/h2-3H,1H2
| Molecular Formula | CH4S2 |
| Molecular Weight | 80.172 |
| 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 |
|---|---|---|
| Indium complexes supported by 1,omega-dithiaalkanediyl-bridged bis(phenolato) ligands: synthesis, structure, and controlled ring-opening polymerization of L-lactide. | 2009-06-15 |
|
| Does s-methyl methanethiosulfonate trap the thiol-disulfide state of proteins? | 2007-04 |
|
| A selective AT2 receptor ligand with a gamma-turn-like mimetic replacing the amino acid residues 4-5 of angiotensin II. | 2004-02-12 |
|
| Synthesis and biological activity of new quinoxaline antibiotics of echinomycin analogues. | 2004-01-19 |
|
| meso-Bis(phenylsulfinyl)methane. | 2003-05 |
|
| Synthesis, receptor binding affinities and conformational properties of cyclic methylenedithioether analogues of angiotensin II. | 2001-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:01:58 GMT 2025
by
admin
on
Mon Mar 31 19:01:58 GMT 2025
|
| Record UNII |
LSC543N4PH
|
| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
DIMERCAPTOMETHANE
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1649
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138818
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DTXSID50217580
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LSC543N4PH
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6725-64-0
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