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177814

Sigma-Aldrich

1,1,1-Trifluoro-2-iodoethane

99%

Synonym(s):

2,2,2-Trifluoroethyl iodide, 2-Iodo-1,1,1-trifluoroethane

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About This Item

Linear Formula:
CF3CH2I
CAS Number:
353-83-3
Molecular Weight:
209.94
Beilstein:
1733201
EC Number:
206-541-0
MDL number:
MFCD00001082
UNSPSC Code:
12352100
PubChem Substance ID:
24850691
NACRES:
NA.22

vapor pressure

3.96 psi ( 20 °C)

Assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.401 (lit.)

bp

54.8 °C (lit.)

density

2.13 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

FC(F)(F)CI

InChI

1S/C2H2F3I/c3-2(4,5)1-6/h1H2

InChI key

RKOUFQLNMRAACI-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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)

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Apeng Liang et al.
Chemical communications (Cambridge, England), 48(66), 8273-8275 (2012-07-13)
The cross-coupling reactions of 1,1,1-trifluoro-2-iodoethane with aryl and heteroaryl boronic acid esters have been successfully achieved. The new protocol allows for a convenient introduction of trifluoroethyl groups into a variety of aryl and heteroaryl moieties under mild conditions.
M P Bouche et al.
Clinical chemistry, 47(2), 281-291 (2001-02-13)
During low-flow or closed-circuit anesthesia with the fluorinated inhalation anesthetic sevoflurane, compound A, an olefinic degradation product with known nephrotoxicity in rats, is generated on contact with alkaline CO(2) adsorbents. To evaluate compound A formation and thus potential sevoflurane toxicity
Roberto Morales-Cerrada et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(1), 296-308 (2018-09-20)
Thermal decarbonylation of the acyl compounds [Mn(CO)5 (CORF )] (RF =CF3 , CHF2 , CH2 CF3 , CF2 CH3 ) yielded the corresponding alkyl derivatives [Mn(CO)5 (RF )], some of which have not been previously reported. The compounds were fully

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