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Merck
CN

177814

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24850691
EC Number:
206-541-0
Beilstein/REAXYS Number:
1733201
MDL number:
MFCD00001082

Key Documents

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Product Name

1,1,1-Trifluoro-2-iodoethane, 99%

assay

99%

form

liquid

InChI key

RKOUFQLNMRAACI-UHFFFAOYSA-N

InChI

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

SMILES string

FC(F)(F)CI

vapor pressure

3.96 psi ( 20 °C)

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.)

functional group

fluoro
iodo

storage temp.

2-8°C

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB3950
STBL4389
STBK5186
STBJ7465
STBJ7213

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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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