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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
Carbonic anhydrase inhibitors: synthesis of water soluble sulfonamides incorporating a 4-sulfamoylphenylmethylthiourea scaffold, with potent intraocular pressure lowering properties.
2002 Oct
Synthesis of isothiocyanate-derived mercapturic acids.
2003 Jul-Aug
Synthesis and evaluation of 5-Aryl-3-(4-hydroxyphenyl)-1,3,4-oxadiazole-2-(3H)-thiones as P-glycoprotein inhibitors.
2003 Jun
Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices.
2004 Dec 3
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 Dec 6
Targeted delivery of a triplex-forming oligonucleotide to hepatic stellate cells.
2005 Mar 22
Radioiodinated azide and isothiocyanate derivatives of cocaine for irreversible labeling of dopamine transporters: synthesis and covalent binding studies.
2005 May-Jun
Identification and distribution of heparan sulfate proteoglycans in the white muscle of Atlantic cod (Gadus morhua) and spotted wolffish (Anarhichas minor).
2006 Apr
Thioureido N-acetyllactosamine derivatives as potent galectin-7 and 9N inhibitors.
2006 Feb 15
An optical-optical double resonance probe of the lowest triplet state of jet-cooled thiophosgene: rovibronic structures and electronic relaxation.
2006 Mar 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 Mar 7
Enhanced A3 adenosine receptor selectivity of multivalent nucleoside-dendrimer conjugates.
2008 Oct 23
Rotational level involvement in the T1-->S0 intersystem crossing transition in thiophosgene.
2009 Apr 7
Capsaicinoids, chloropicrin and sulfur mustard: possibilities for exposure biomarkers.
2010
Carcinogenic mode of action of folpet in mice and evaluation of its relevance to humans.
2010 Jul
The Fock space method of vibrational analysis.
2010 Jun 21
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:38:38 GMT 2023
Edited
by admin
on Fri Dec 15 18:38:38 GMT 2023
Record UNII
067FQP576P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
THIOPHOSGENE
HSDB  
Systematic Name English
CARBONOTHIOIC DICHLORIDE
Systematic Name English
THIOPHOSGENE [HSDB]
Common Name English
THIOCARBONYL CHLORIDE
Systematic Name English
Code System Code Type Description
CAS
463-71-8
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
PRIMARY
HSDB
861
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
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PUBCHEM
10040
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-341-6
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
PRIMARY
FDA UNII
067FQP576P
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID2060046
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
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MESH
C016145
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
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CHEBI
29366
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
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WIKIPEDIA
THIOPHOSGENE
Created by admin on Fri Dec 15 18:38:38 GMT 2023 , Edited by admin on Fri Dec 15 18:38:38 GMT 2023
PRIMARY