Skip to Content
Merck
All Photos(1)

Key Documents

510254

Sigma-Aldrich

Ethyl 3,3,3-trifluoropyruvate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CF3COCO2C2H5
CAS Number:
Molecular Weight:
170.09
Beilstein:
2087388
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.341 (lit.)
n/D (lit.)

density

1.283 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)C(=O)C(F)(F)F

InChI

1S/C5H5F3O3/c1-2-11-4(10)3(9)5(6,7)8/h2H2,1H3

InChI key

KJHQVUNUOIEYSV-UHFFFAOYSA-N

Related Categories

General description

Ethyl 3,3,3-trifluoropyruvate is a trifluoromethylated compound. Enantioselective Friedel–Crafts alkylation of simple phenols and indoles with ethyl 3,3,3-trifluoropyruvate under different reaction conditions have been reported.

Application

Ethyl 3,3,3-trifluoropyruvate may be used in the preparation of N-heteroaryl(trifluoromethyl)hydroxyalkanoic acid esters.

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31 °C - closed cup

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis of N-Heteroaryl (trifluoromethyl) hydroxyalkanoic Acid Esters by Highly Efficient Solid Acid-Catalyzed Hydroxyalkylation of Indoles and Pyrroles with Activated Trifluoromethyl Ketones.
Abid M and Torok B.
Advanced Synthesis & Catalysis, 347(14), 1797-1803 (2005)
Organocatalytic enantioselective Friedel?Crafts alkylation of simple phenols with trifluoropyruvate.
Zhao JL, et al.
Tetrahedron Letters, 49(9), 1476-1479 (2008)
Novel Enantiocomplementary C2-Symmetric Chiral Bis (imidazoline) Ligands: Highly Enantioselective Friedel?Crafts Alkylation of Indoles with Ethyl 3, 3, 3-Trifluoropyruvate.
Nakamura S, et al.
Advanced Synthesis & Catalysis, 350(10), 1443-1448 (2008)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service