Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH2S3 |
| Molecular Weight | 110.222 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
SC(S)=S
InChI
InChIKey=HIZCIEIDIFGZSS-UHFFFAOYSA-N
InChI=1S/CH2S3/c2-1(3)4/h(H2,2,3,4)
| Molecular Formula | CH2S3 |
| Molecular Weight | 110.222 |
| 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 |
|---|---|---|
| Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anions. | 2009 Apr 1 |
|
| Thermoresponsive nanohydrogels cross-linked by gold nanoparticles. | 2010 Aug |
|
| Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II-trithiocarbonate adduct--an inhibitor mimicking the sulfonamide and urea binding to the enzyme. | 2010 Jan 15 |
|
| Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamate. | 2010 Mar 1 |
|
| New formation mechanism of allylic trithiocarbonates from sodium O-(2-Alkenyl) dithiocarbonates via sequential pericyclic reactions: Density functional theory study. | 2010 Nov |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:16:39 UTC 2023
by
admin
on
Fri Dec 15 15:16:39 UTC 2023
|
| Record UNII |
O27JHO40J8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
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| Code System | Code | Type | Description | ||
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Thiocarbonic acid
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DTXSID00862140
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594-08-1
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36967
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209-822-6
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O27JHO40J8
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68982
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m11206
Created by
admin on Fri Dec 15 15:16:39 UTC 2023 , Edited by admin on Fri Dec 15 15:16:39 UTC 2023
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PRIMARY | Merck Index |