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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)

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’.

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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
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.
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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