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About This Item
Linear Formula:
CH3COOCH2CCl3
CAS Number:
Molecular Weight:
191.44
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1757888
Assay:
≥98.0% (GC)
InChI
1S/C4H5Cl3O2/c1-3(8)9-2-4(5,6)7/h2H2,1H3
SMILES string
CC(=O)OCC(Cl)(Cl)Cl
InChI key
XHAXVDWUMCHTCY-UHFFFAOYSA-N
assay
≥98.0% (GC)
refractive index
n20/D 1.457
density
1.401 g/mL at 20 °C (lit.)
General description
2,2,2-Trichloroethyl acetate is used as acetyl donor in anhydrous, enzyme-catalyzed enantioselective acetylations.
Application
2,2,2-Trichloroethyl acetate may be used in the enzyme catalyzed synthesis of enantiomerically pure prostaglandin intermediate, (1S,4R)-(-)-4-hydroxy-2-cyclopentenyl acetate.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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F. Theil et al.
Synthesis, 540-540 (1988)
Synthesis of (1S, 4R)-(-)-4-Hydroxy-2-cyclopentenyl Acetate by a Highly Enantioselective Enzyme-Catalyzed Transesterification in Organic Solvents
Theil F, et al.
Synthesis, 07, 540-541 (1988)
M.A. Djadchenko et al.
Journal of the Chemical Society. Perkin Transactions 1, 2001-2001 (1989)
G. Carrea et al.
Journal of the Chemical Society. Perkin Transactions 1, 1057-1057 (1989)
M. Therisod et al.
Journal of the American Chemical Society, 108, 5638-5638 (1986)
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