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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
Structure of THIOFORMAMIDE

SMILES

NC=S

InChI

InChIKey=CYEBJEDOHLIWNP-UHFFFAOYSA-N
InChI=1S/CH3NS/c2-1-3/h1H,(H2,2,3)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
1-(4-Bromo-phen-yl)-3-butano-ylthio-urea.
2010-12-08
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.
2010-11-15
Bis(carbonyl-κC)(N,N-dimethyl-thio-carbamoyl-κC,S)(pyridine-2-thiol-ato-κN,S)(triphenyl-phosphine-κP)molybdenum(II).
2010-09-04
Peptide-catalyzed kinetic resolution of formamides and thioformamides as an entry to nonracemic amines.
2010-03-10
Synthesis and antibacterial activity of some new thiazole and thiophene derivatives.
2009-11
Sequential addition reactions of two molecules of Grignard reagents to thioformamides.
2009-08-07
Mercury sorption on a thiocarbamoyl derivative of chitosan.
2009-06-15
Unusually high enantioselectivity in high-performance liquid chromatography using cellulose tris(4-methylbenzoate) as a chiral stationary phase.
2009-05-29
Covalent modification of lysine residues by allyl isothiocyanate in physiological conditions: plausible transformation of isothiocyanate from thiol to amine.
2009-03-16
Synthesis and molluscicidal activity of some new thiophene, thiadiazole and pyrazole derivatives.
2009-03
Bis-pyrazolines: synthesis, characterization and antiamoebic activity as inhibitors of growth of Entamoeba histolytica.
2009-01
LC/MS/MS Analysis of N-Terminal Protein Adducts with Improved Sensitivity: A Comparison of Selected Edman Isothiocyanate Reagents.
2009
Recent improvements in the development of A(2B) adenosine receptor agonists.
2008-12
New Pd(II) complexes of the synthesized 1-N-substituted thiosemicarbazones of 3-indole carboxaldehyde: characterization and antiamoebic assessment against E. histolytica.
2008-09
Dichloridotriphenyl-anti-mony(V)-bis-(pyrrolidin-1-ylthio-carbon-yl) disulfide (1/1).
2007-12-06
Two-state model based on the block-localized wave function method.
2007-06-14
Synthesis and fluorescent properties of bi- and tricyclic 4-N-carbamoyldeoxycytidine derivatives.
2007-01-05
Lower-rim substituted calixarenes and their applications.
2007
Hypervalent iodine mediated intramolecular cyclization of thioformanilides: expeditious approach to 2-substituted benzothiazoles.
2006-10-13
First-principles calculation of geometry and anharmonic vibrational spectra of thioformamide and thioformamide-d2.
2006-01-07
Structure-activity relationships of K(ATP) channel openers.
2006
Synthesis of some new 5-(2-substituted-1,3-thiazol-5-yl)-2-hydroxy benzamides and their 2-alkoxy derivatives as possible antifungal agents.
2004-10
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.
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:03 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:03 GMT 2025
Record UNII
G525TLN0E7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIOFORMAMIDE [MI]
Preferred Name English
THIOFORMAMIDE
MI  
Systematic Name English
METHANETHIOAMIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
3005587
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID00150918
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
CAS
115-08-2
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
MESH
C009463
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
MERCK INDEX
m10756
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
204-063-7
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
FDA UNII
G525TLN0E7
Created by admin on Mon Mar 31 18:52:03 GMT 2025 , Edited by admin on Mon Mar 31 18:52:03 GMT 2025
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS