U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C3Cl6O3
Molecular Weight 296.748
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRIPHOSGENE

SMILES

ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl

InChI

InChIKey=UCPYLLCMEDAXFR-UHFFFAOYSA-N
InChI=1S/C3Cl6O3/c4-2(5,6)11-1(10)12-3(7,8)9

HIDE SMILES / InChI

Molecular Formula C3Cl6O3
Molecular Weight 296.748
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Debenzylation of tertiary amines using phosgene or triphosgene: an efficient and rapid procedure for the preparation of carbamoyl chlorides and unsymmetrical ureas. Application in carbon-11 chemistry.
2003 Sep 19
Synthesis of disubstituted imidazo[4,5-b]pyridin-2-ones.
2004 Oct 29
Development of an efficient strategy for the synthesis of the ETB receptor antagonist BQ-788 and some related analogues.
2005 Aug
Deazapurine solid-phase synthesis: combinatorial synthesis of a library of N3,N5,C6-trisubstituted pyrrolo[3,2-d]pyrimidine derivatives on cross-linked polystyrene bearing a cysteamine linker.
2005 Nov-Dec
Peptide crosslinked micelles: a new strategy for the design and synthesis of peptide vaccines.
2006
Synthesis of hydantoins from enantiomerically pure alpha-amino amides without epimerization.
2006 Feb 17
Peptide immobilization on amine-terminated boron-doped diamond surfaces.
2007 Apr 10
[Emergency treatment and nursing for patients with acute triphosgene poisoning].
2007 Mar
Gold(I) chloride adducts of 1,3-bis(di-2-pyridylphosphino)propane: synthesis, structural studies and antitumour activity.
2007 Nov 21
Intracerebroventricular administration of N-acetylaspartylglutamate (NAAG) peptidase inhibitors is analgesic in inflammatory pain.
2008 Aug 1
Synthesis and in silico biological activity evaluation of new N-substituted pyrazolo-oxazin-2-one systems.
2008 Mar 15
Synthesis and biological evaluation of a novel pentagastrin-toxin conjugate designed for a targeted prodrug mono-therapy of cancer.
2008 May
Simple, rapid, and highly sensitive detection of diphosgene and triphosgene by spectrophotometric methods.
2009 Nov 15
Novel synthesis of N-alkoxycarbonyl amino acids and surfactant properties of their sodium salts.
2010
Inhibitors of N(alpha)-acetyl-L-ornithine deacetylase: synthesis, characterization and analysis of their inhibitory potency.
2010 Apr
6-Chloro-8-methyl-4H-3,1-benzoxazine-2,4(1H)-dione.
2010 Apr 21
Solid phase synthesis of hydrogen bond surrogate derived alpha-helices: resolving the case of a difficult amide coupling.
2010 Apr 21
Prostate apoptosis response protein 4 sensitizes human colon cancer cells to chemotherapeutic 5-FU through mediation of an NF kappaB and microRNA network.
2010 Apr 30
Oriented synthesis and in vitro anticancer activity of biquinazoline-2,2'-diones.
2010 Jan-Feb
catena-Poly[[[triaqua-sulfatozinc(II)]-μ-3,3'-bis-(3-pyrid-yl)-1,1'-(m-phenyl-ene)diurea] methanol solvate monohydrate].
2010 Mar 17
In vitro and in vivo studies of the trypanocidal properties of WRR-483 against Trypanosoma cruzi.
2010 Sep 14
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:53:12 GMT 2023
Edited
by admin
on Sat Dec 16 02:53:12 GMT 2023
Record UNII
2C0677Q3B2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIPHOSGENE
MI  
Systematic Name English
TRIPHOSGENE [MI]
Common Name English
HEXACHLORODIMETHYL CARBONATE
Common Name English
TRICHLOROMETHYL CARBONATE
Systematic Name English
BTC
Common Name English
CARBONIC ACID, BIS(TRICHLOROMETHYL) ESTER
Common Name English
BIS(TRICHLOROMETHYL) CARBONATE
Systematic Name English
METHANOL, TRICHLORO-, CARBONATE (2:1)
Systematic Name English
1,1,1-TRICHLOROMETHANOL 1,1'-CARBONATE
Common Name English
Code System Code Type Description
WIKIPEDIA
TRIPHOSGENE
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
MERCK INDEX
m11191
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY Merck Index
SMS_ID
100000164210
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
FDA UNII
2C0677Q3B2
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
PUBCHEM
94429
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
EVMPD
SUB178573
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
CAS
32315-10-9
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
250-986-3
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID00865631
Created by admin on Sat Dec 16 02:53:12 GMT 2023 , Edited by admin on Sat Dec 16 02:53:12 GMT 2023
PRIMARY