15217
Bis(trichloromethyl) carbonate
purum, ≥99.0% (AT)
Synonym(s):
Triphosgene, tri-Phosgene
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About This Item
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grade
purum
Assay
≥99.0% (AT)
form
solid
mp
77-82 °C
functional group
carbonate
storage temp.
2-8°C
SMILES string
ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl
InChI
1S/C3Cl6O3/c4-2(5,6)11-1(10)12-3(7,8)9
InChI key
UCPYLLCMEDAXFR-UHFFFAOYSA-N
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Application
Bis(trichloromethyl) carbonate was used in the preparation of Fmoc-amino acid chlorides. It was also used in the preparation of aryl-(Z)-vinyl chlorides.
Other Notes
Crystalline, easy-to-handle substitute for phosgene; 1 mole of the reagent corresponds in its reactivity to 3 moles phosgene
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 1 Inhalation - Skin Corr. 1B
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tetrahedron Letters, 30, 3229-3229 (1989)
Angewandte Chemie (International Edition in English), 99, 922-922 (1987)
Spec. Chem., 14, 357-357 (1994)
Synthetic Communications, 21, 285-285 (1991)
The Journal of organic chemistry, 71(4), 1750-1753 (2006-02-14)
A method for the preparation of enantiomerically pure hydantoins from optically pure alpha-amino amides utilizing triphosgene is described. We also propose that the racemization observed with 1,1'-carbonyldiimidazole (CDI) for this type of reaction is due to the imidazole carbamate intermediates.
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