2,2,2-trifluoroethyl butyrate

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Names

[ CAS No. ]:
371-27-7

[ Name ]:
2,2,2-trifluoroethyl butyrate

[Synonym ]:
MFCD00077609
Butyric Acid 2,2,2-Trifluoroethyl Ester
2,2,2-Trifluoroethyl Butyrate
2,2,2-trifluoroethyl butanoate

Chemical & Physical Properties

[ Density]:
1.127 g/mL at 25 °C(lit.)

[ Boiling Point ]:
113 °C747 mm Hg(lit.)

[ Melting Point ]:
18°C(lit.)

[ Molecular Formula ]:
C6H9F3O2

[ Molecular Weight ]:
170.13000

[ Flash Point ]:
75 °F

[ Exact Mass ]:
170.05500

[ PSA ]:
26.30000

[ LogP ]:
1.89200

[ Index of Refraction ]:
n20/D 1.347(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H315-H319-H335

[ Precautionary Statements ]:
P210-P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
UN 3272 3/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
3.2

Articles

Solvent effects in lipase-catalysed transesterification reactions.

Acta Chem. Scand. 44(10) , 1032-5, (1990)

Porcine pancreatic lipase-catalysed transesterifications of 2,2,2-trifluoroethyl butyrate with racemic 2-octanol and 1-phenylethanol have been studied in different organic solvents. Solvent hydrophobi...

Asymmetric strecker synthesis of alpha-amino acids via a crystallization-induced asymmetric transformation using (R)-phenylglycine amide as chiral auxiliary.

Org. Lett. 3(8) , 1121-4, (2001)

[reaction: see text]. Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are reported. The Strecker reaction is accompanied by an in situ crystallization-induce...

Lipase catalysis in the optical resolution of 2-amino-1-phenylethanol derivatives. Kanerva LT, et al.

J. Chem. Soc. Perkin Trans. I 14 , 1759-1762., (1992)


More Articles


Related Compounds

  • 2,2,2-trifluoroethyl N-(4-nitrophenyl)carbamate
  • 2,2,2-trifluoroethyl (3S)-3-acetamidobutanoate
  • 2,2,2-trifluoroethyl acetyl-L-phenylalaninate
  • 2,2,2-trifluoroethyl 1-chloroacetate
  • 2,2,2-Trifluoroethyl methacrylate
  • 2,2,2-trifluoroethyl 2-(N-ethyl-4-formyl-3-methylanilino)acetate