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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

Unknown
139594
PubMed

PubMed

TitleDatePubMed
A novel strategy for the synthesis of neoglycoconjugates from deacylated deep rough lipopolysaccharides.
2002
Carbonic anhydrase inhibitors: synthesis of water soluble sulfonamides incorporating a 4-sulfamoylphenylmethylthiourea scaffold, with potent intraocular pressure lowering properties.
2002 Oct
Synthesis of neoglycoproteins containing O-methylated trisaccharides related to excretory/secretory antigens of Toxocara larvae.
2003 Jan 2
Synthesis and evaluation of 5-Aryl-3-(4-hydroxyphenyl)-1,3,4-oxadiazole-2-(3H)-thiones as P-glycoprotein inhibitors.
2003 Jun
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
Symmetry segregation of the vibronic levels within the S1<--S0 system of thiophosgene, Cl2CS, by optical-optical double resonance spectroscopy.
2007 Apr 14
Synthesis of alpha- and beta-glycosyl isothiocyanates via oxazoline intermediates.
2007 Jun 8
Capsaicinoids, chloropicrin and sulfur mustard: possibilities for exposure biomarkers.
2010
Patents

Patents

03991071
1
04099003
2
04107201
1
04144341
4
04154945
1
04294919
2
04424213
5
04460587
1
04521242
2
04599203
1
04707488
1
04876266
1
04877723
2
04968720
1
04988689
4
05126339
2
05134144
5
05232826
1
05246935
1
05290795
1
05424443
1
05616706
8
05681833
1
05798374
1
05883110
1
05977154
6
06011053
1
06080772
2
06159998
5
06166208
3
06248306
2
06716491
1
06906063
2
07115640
4
07138421
2
07338959
2
07348354
1
07495009
2
07652023
2
07795256
1
07935819
6
07947721
3
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
PRIMARY
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
NIH
NCATS
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