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274259

Sigma-Aldrich

Methyl P,P-bis(2,2,2-trifluoroethyl)phosphonoacetate

95%

Synonym(s):

Bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate

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About This Item

Linear Formula:
CH3O2CCH2P(O)(OCH2CF3)2
CAS Number:
Molecular Weight:
318.11
Beilstein:
3594044
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

liquid

reaction suitability

reaction type: C-C Bond Formation

refractive index

n20/D 1.370 (lit.)

density

1.504 g/mL at 25 °C (lit.)

functional group

ester
fluoro
phosphonate

SMILES string

COC(=O)CP(=O)(OCC(F)(F)F)OCC(F)(F)F

InChI

1S/C7H9F6O5P/c1-16-5(14)2-19(15,17-3-6(8,9)10)18-4-7(11,12)13/h2-4H2,1H3

InChI key

PVSJXEDBEXYLML-UHFFFAOYSA-N

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Application

Methyl P,P-bis(2,2,2-trifluoroethyl)phosphonoacetate can be used:
  • In one of the key synthetic steps for the preparation of trans-hydrindanes and (R)-(+)-umbelactone.
  • To prepare a cis-olefinic ester derivative by Still–Gennari olefination of an aldehyde derivative using 18-crown ether and potassium bis(trimethylsilyl)amide (KHMDS).
  • In the synthesis of (−)-(6S,2′S)-epi cryptocaryalactone.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

274259-5G:
274259-1G:
274259-VAR:
274259-BULK:


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Sulfur-mediated intramolecular double Michael-type reaction: synthesis of trans-hydroindanes and mechanism
Ihara M, et al.
Journal of the Chemical Society. Perkin Transactions 1, 19, 2527-2535 (1992)
Journal of the Chemical Society. Perkin Transactions 1, 2527-2527 (1992)
Stereoselective total synthesis of (+)-(6R, 2′S)-cryptocaryalactone and (−)-(6S, 2′S)-epi cryptocaryalactone
Sabitha G, et al.
Tetrahedron, 64(44), 10207-10213 (2008)
First stereoselective total synthesis of pectinolide H
Ramesh D, et al.
Tetrahedron Letters, 53(10), 1258-1260 (2012)

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