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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

Approval Year

PubMed

PubMed

TitleDatePubMed
Selective cleavage of N-benzyl-protected secondary amines by triphosgene.
2003 Jan 24
Parallel solid-phase synthesis of disubstituted (5-biphenyltetrazolyl) hydantoins and thiohydantoins targeting the growth hormone secretagogue receptor.
2004 Jan 19
The use of solid-phase supported 1-N-piperazine-4-N-carboxaldehyde in Vilsmeier reactions.
2004 Mar-Apr
Novel fluoro- and hydroxyl-containing jasmonate derivatives as highly efficient elicitors in suspension cultures of Taxus chinensis.
2004 Sep 20
Synthesis of hydantoins from enantiomerically pure alpha-amino amides without epimerization.
2006 Feb 17
Gold(I) chloride adducts of 1,3-bis(di-2-pyridylphosphino)propane: synthesis, structural studies and antitumour activity.
2007 Nov 21
Pharmacokinetic characteristics and anticancer effects of 5-fluorouracil loaded nanoparticles.
2008 Apr 15
The Amadori rearrangement as key reaction for the synthesis of neoglycoconjugates.
2008 Aug 11
Cyclization of hydrazones of 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene. Synthesis of Spiro naphthoxazine dimers.
2009 Jun 12
Solid phase synthesis of hydrogen bond surrogate derived alpha-helices: resolving the case of a difficult amide coupling.
2010 Apr 21
Synthesis of 1,3-azaphosphol-2-ones. Crystal and molecular structures of [SP-4-2]-dichlorobis(3-phenyl-1,3-dihydrobenzo[1,3]azaphosphol-2-one-P)palladium(II) and its chloro(methyl)platinum(II) analogue.
2010 Jan 7
catena-Poly[[[triaqua-sulfatozinc(II)]-μ-3,3'-bis-(3-pyrid-yl)-1,1'-(m-phenyl-ene)diurea] methanol solvate monohydrate].
2010 Mar 17
Patents
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