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Details

Stereochemistry ACHIRAL
Molecular Formula CCl2S
Molecular Weight 114.982
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIOPHOSGENE

SMILES

ClC(Cl)=S

InChI

InChIKey=ZWZVWGITAAIFPS-UHFFFAOYSA-N
InChI=1S/CCl2S/c2-1(3)4

HIDE SMILES / InChI

Molecular Formula CCl2S
Molecular Weight 114.982
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Carcinogenic mode of action of folpet in mice and evaluation of its relevance to humans.
2010-07
The Fock space method of vibrational analysis.
2010-06-21
Thermal decomposition of captan and formation pathways of toxic air pollutants.
2010-06-01
[Construction of recombinant adenovirus vector pAdxsi-green fluorescent protein-homo sapiens NEL-like 1 and transfected into rat bone marrow mesenchymal stem cells].
2010-05
Capsaicinoids, chloropicrin and sulfur mustard: possibilities for exposure biomarkers.
2010
Bis(2,2'-bipyridine)(5-isothio-cyanato-1,10-phenanthroline)ruthenium(II) bis-(hexa-fluoridophosphate) acetonitrile solvate.
2009-09-09
Synthesis and antitumor activity of optically active thiourea and their 2-aminobenzothiazole derivatives: a novel class of anticancer agents.
2009-07
Rotational level involvement in the T1-->S0 intersystem crossing transition in thiophosgene.
2009-04-07
Amine-reactive fluorene probes: synthesis, optical characterization, bioconjugation, and two-photon fluorescence imaging.
2008-12
Enhanced A3 adenosine receptor selectivity of multivalent nucleoside-dendrimer conjugates.
2008-10-23
Constructing the OCF2O moiety using BrF3.
2008-09-05
A combined theoretical treatment of T(1)-->S(0) intersystem crossing and intramolecular vibrational redistribution in thiophosgene.
2008-03-07
Physicochemical characteristics and bronchial epithelial cell cytotoxicity of Folpan 80 WG(R) and Myco 500(R), two commercial forms of folpet.
2007-09-20
Synthesis of alpha- and beta-glycosyl isothiocyanates via oxazoline intermediates.
2007-06-08
Symmetry segregation of the vibronic levels within the S1<--S0 system of thiophosgene, Cl2CS, by optical-optical double resonance spectroscopy.
2007-04-14
Assignment and extraction of dynamics of a small molecule with a complex vibrational spectrum: thiophosgene.
2006-04-27
Identification and distribution of heparan sulfate proteoglycans in the white muscle of Atlantic cod (Gadus morhua) and spotted wolffish (Anarhichas minor).
2006-04
An optical-optical double resonance probe of the lowest triplet state of jet-cooled thiophosgene: rovibronic structures and electronic relaxation.
2006-03-28
Isomers among the carbon sulfides C4S6--synthesis and crystal structures of alpha,alpha-C4S6, alpha,beta-C4S6, and of a second polymorph of the diiodine adduct alpha,beta-C4S6.I2.
2006-03-07
Thioureido N-acetyllactosamine derivatives as potent galectin-7 and 9N inhibitors.
2006-02-15
Radioiodinated azide and isothiocyanate derivatives of cocaine for irreversible labeling of dopamine transporters: synthesis and covalent binding studies.
2005-05-19
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds.
2005-05-02
Targeted delivery of a triplex-forming oligonucleotide to hepatic stellate cells.
2005-03-22
Striving to understand the photophysics and photochemistry of thiophosgene: a combined CASSCF and MR-CI study.
2005-02-03
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides derived from 4-isothiocyanato-benzolamide.
2004-12-06
Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices.
2004-12-03
Insights into dynamics of the S2 state of thiophosgene from ab initio calculations.
2004-10-08
S(1S) production following electron impact on thiophosgene (Cl2CS).
2004-05-15
A new bifunctional chelating agent conjugated with monoclonal antibody and labelled with technetium-99m for targeted scintigraphy: 6-(4-isothiocyanatobenzyl)-5,7-dioxo-1,11-(carboxymethyl)-1,4,8,11-tetraazacyclotridecane.
2004
Synthesis of N-benzyl- and N-phenyl-2-amino-4,5-dihydrothiazoles and thioureas and evaluation as modulators of the isoforms of nitric oxide synthase.
2003-09-15
Synthesis of isothiocyanate-derived mercapturic acids.
2003-08-23
Synthesis and evaluation of 5-Aryl-3-(4-hydroxyphenyl)-1,3,4-oxadiazole-2-(3H)-thiones as P-glycoprotein inhibitors.
2003-06
Synthesis of neoglycoproteins containing O-methylated trisaccharides related to excretory/secretory antigens of Toxocara larvae.
2003-01-02
Carbonic anhydrase inhibitors: synthesis of water soluble sulfonamides incorporating a 4-sulfamoylphenylmethylthiourea scaffold, with potent intraocular pressure lowering properties.
2002-10
A novel bornane synthesis by an old idea.
2002-05-31
A novel strategy for the synthesis of neoglycoconjugates from deacylated deep rough lipopolysaccharides.
2002
Isolation of highly infectious and pure adeno-associated virus type 2 vectors with a single-step gravity-flow column.
2001-01-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:49 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:49 GMT 2025
Record UNII
067FQP576P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIOPHOSGENE [HSDB]
Preferred Name English
THIOPHOSGENE
HSDB  
Systematic Name English
CARBONOTHIOIC DICHLORIDE
Systematic Name English
THIOCARBONYL CHLORIDE
Systematic Name English
Code System Code Type Description
CAS
463-71-8
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
HSDB
861
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
PUBCHEM
10040
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-341-6
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
FDA UNII
067FQP576P
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID2060046
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
MESH
C016145
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
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CHEBI
29366
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY
WIKIPEDIA
THIOPHOSGENE
Created by admin on Mon Mar 31 19:17:50 GMT 2025 , Edited by admin on Mon Mar 31 19:17:50 GMT 2025
PRIMARY