Skip to content
2,2,2-trifluoroethanol

Structure via PubChem · Public domain (PubChem)

EntityQ2474643· pop 21· linked from 701 articles

2,2,2-trifluoroethanol

Sign in to save

Also known as 2,2,2-trifluoroethyl alcohol, TFE, trifluoroethanol

2,2,2-Trifluoroethanol is the synthetic organic compound with the formula CF3CH2OH. Also known as TFEA or trifluoroethyl alcohol, this colourless, water-miscible liquid has a smell reminiscent of ethanol. Due to the electronegativity of the trifluoromethyl group, this alcohol exhibits a stronger acidic character compared to ethanol.

In the Vinony graph

Within Vinony's link graph, 2,2,2-trifluoroethanol is referenced by 701 other articles, and connects out to ginkgolide, picrotoxin and benzodiazepine drug.

It is catalogued under topics including Chembox having GHS data, Chembox image size set and Chemical articles with multiple compound IDs.

Its subject is documented across 20 Wikipedia language editions.

Chemical data

Formula
C2H3F3O
Molecular weight
100.04 g/mol
IUPAC name
2,2,2-trifluoroethanol
SMILES
C(C(F)(F)F)O
InChIKey
RHQDFWAXVIIEBN-UHFFFAOYSA-N
XLogP
0.4
Polar surface area
20.2 Ų
H-bond donors
1
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of
primary alcohol
Has part
carbon
Mass
100.014
Show 6 more facts
chemical formula
C₂H₃F₃O
pKa
12.37
canonical SMILES
C(C(F)(F)F)O
global warming potential
24
melting point
-44
Commons category
2,2,2-Trifluoroethanol
Sources (2)

via Wikidata · CC0

~3 min read

Encyclopedic overview

7 sections
Contents
  • Synthesis
  • Properties
  • Reactions
  • Safety
  • See also
  • References
  • External links

2,2,2-Trifluoroethanol is the synthetic organic compound with the formula CF3CH2OH. Also known as TFEA or trifluoroethyl alcohol, this colourless, water-miscible liquid has a smell reminiscent of ethanol. Due to the electronegativity of the trifluoromethyl group, this alcohol exhibits a stronger acidic character compared to ethanol.

==Synthesis== Trifluoroethanol is produced industrially by hydrogenation or the hydride reduction of derivatives of trifluoroacetic acid, such as the esters or acyl chloride.

Excerpted from Wikipedia’s “2,2,2-trifluoroethanol” article, available under the CC BY-SA 4.0 licence.

Connections

Categories