Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH3NS.H2O |
| Molecular Weight | 79.122 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.NC=S
InChI
InChIKey=ASRARIHEARHGOW-UHFFFAOYSA-N
InChI=1S/CH3NS.H2O/c2-1-3;/h1H,(H2,2,3);1H2
| 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 |
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| 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 |
|---|---|---|
| R(-)-4-(3-Isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole, a fluorescent chiral tagging reagent: sensitive resolution of chiral amines and amino acids by reversed-phase liquid chromatography. | 2001 Feb |
|
| Synthesis of some new 5-(2-substituted-1,3-thiazol-5-yl)-2-hydroxy benzamides and their 2-alkoxy derivatives as possible antifungal agents. | 2004 Oct |
|
| New Pd(II) complexes of the synthesized 1-N-substituted thiosemicarbazones of 3-indole carboxaldehyde: characterization and antiamoebic assessment against E. histolytica. | 2008 Sep |
|
| Mercury sorption on a thiocarbamoyl derivative of chitosan. | 2009 Jun 15 |
|
| Synthesis and antibacterial activity of some new thiazole and thiophene derivatives. | 2009 Nov |
|
| 1-(4-Bromo-phen-yl)-3-butano-ylthio-urea. | 2010 Dec 8 |
|
| Sulfur-containing compounds quench 3,7-dihydro-2-methyl-6-(4-methoxyphenyl)imidazol[1,2-a]pyrazine-3-one chemiluminescence: Discrimination between true antioxidants and quenchers using xanthine oxidase. | 2010 Nov 15 |
|
| Bis(carbonyl-κC)(N,N-dimethyl-thio-carbamoyl-κC,S)(pyridine-2-thiol-ato-κN,S)(triphenyl-phosphine-κP)molybdenum(II). | 2010 Sep 4 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:21:44 GMT 2023
by
admin
on
Sat Dec 16 08:21:44 GMT 2023
|
| Record UNII |
2AZD49JS7J
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| Record Status |
Validated (UNII)
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| Record Version |
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| Related Record | Type | Details | ||
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ANHYDROUS->SOLVATE |
