Details
Stereochemistry | ACHIRAL |
Molecular Formula | CH3NS |
Molecular Weight | 61.106 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC=S
InChI
InChIKey=CYEBJEDOHLIWNP-UHFFFAOYSA-N
InChI=1S/CH3NS/c2-1-3/h1H,(H2,2,3)
Molecular Formula | CH3NS |
Molecular Weight | 61.106 |
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 |
---|---|---|
Structure-activity relationships of K(ATP) channel openers. | 2006 |
|
First-principles calculation of geometry and anharmonic vibrational spectra of thioformamide and thioformamide-d2. | 2006 Jan 7 |
|
Lower-rim substituted calixarenes and their applications. | 2007 |
|
Dichloridotriphenyl-anti-mony(V)-bis-(pyrrolidin-1-ylthio-carbon-yl) disulfide (1/1). | 2007 Dec 6 |
|
Synthesis and fluorescent properties of bi- and tricyclic 4-N-carbamoyldeoxycytidine derivatives. | 2007 Jan 5 |
|
LC/MS/MS Analysis of N-Terminal Protein Adducts with Improved Sensitivity: A Comparison of Selected Edman Isothiocyanate Reagents. | 2009 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:46:15 GMT 2023
by
admin
on
Fri Dec 15 17:46:15 GMT 2023
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Record UNII |
G525TLN0E7
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Record Status |
Validated (UNII)
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Record Version |
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m10756
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Related Record | Type | Details | ||
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SOLVATE->ANHYDROUS |