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About This Item
Linear Formula:
CH3COOCH2CCl3
CAS Number:
Molecular Weight:
191.44
Beilstein:
1757888
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥98.0% (GC)
refractive index
n20/D 1.457
density
1.401 g/mL at 20 °C (lit.)
SMILES string
CC(=O)OCC(Cl)(Cl)Cl
InChI
1S/C4H5Cl3O2/c1-3(8)9-2-4(5,6)7/h2H2,1H3
InChI key
XHAXVDWUMCHTCY-UHFFFAOYSA-N
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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F. Theil et al.
Synthesis, 540-540 (1988)
G. Carrea et al.
Journal of the Chemical Society. Perkin Transactions 1, 1057-1057 (1989)
M.A. Djadchenko et al.
Journal of the Chemical Society. Perkin Transactions 1, 2001-2001 (1989)
M. Therisod et al.
Journal of the American Chemical Society, 108, 5638-5638 (1986)
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)
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