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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
Selective cleavage of N-benzyl-protected secondary amines by triphosgene.
2003 Jan 24
The use of solid-phase supported 1-N-piperazine-4-N-carboxaldehyde in Vilsmeier reactions.
2004 Mar-Apr
Development of an efficient strategy for the synthesis of the ETB receptor antagonist BQ-788 and some related analogues.
2005 Aug
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
Cyclization of hydrazones of 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene. Synthesis of Spiro naphthoxazine dimers.
2009 Jun 12
Highly efficient synthesis of DNA-binding hairpin polyamides via the use of a new triphosgene coupling strategy.
2009 Sep 3
6-Chloro-8-methyl-4H-3,1-benzoxazine-2,4(1H)-dione.
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
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