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MilliporeSigma

419982

Sigma-Aldrich

Triethyl(trifluoromethyl)silane

98%

Synonym(s):

(Trifluoromethyl)triethylsilane, Triethylsilyl trifluoromethane

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1 G
$128.00

$128.00


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About This Item

Linear Formula:
(C2H5)3SiCF3
CAS Number:
Molecular Weight:
184.27
Beilstein/REAXYS Number:
4242161
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22

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Quality Level

assay

98%

form

liquid

reaction suitability

reaction type: C-C Bond Formation

refractive index

n20/D 1.382 (lit.)

bp

56-57 °C/60 mmHg (lit.)

density

0.98 g/mL at 25 °C (lit.)

functional group

fluoro

SMILES string

CC[Si](CC)(CC)C(F)(F)F

InChI

1S/C7H15F3Si/c1-4-11(5-2,6-3)7(8,9)10/h4-6H2,1-3H3

InChI key

ZHSKFONQCREGOG-UHFFFAOYSA-N

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1 of 4

This Item
902489488712367265
assay

98%

assay

≥95%

assay

99%

assay

97%

Quality Level

200

Quality Level

-

Quality Level

200

Quality Level

200

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

-

refractive index

n20/D 1.382 (lit.)

refractive index

n/D 1.496

refractive index

-

refractive index

n20/D 1.488 (lit.)

bp

56-57 °C/60 mmHg (lit.)

bp

-

bp

54-55 °C (lit.)

bp

102-103 °C/0.5 mmHg (lit.)

form

liquid

form

liquid

form

-

form

liquid

Application

Reactant for:
  • Trifluoromethylation of aryl iodides
  • Trialkylsilylation reactions

  • Used for deposition of perfluoro-methyl silica films

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Related product

pictograms

Flame

signalword

Danger

hcodes

pcodes

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

32.0 °F - closed cup

flash_point_c

0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Eun Jin Cho et al.
Science (New York, N.Y.), 328(5986), 1679-1681 (2010-06-26)
The trifluoromethyl group can dramatically influence the properties of organic molecules, thereby increasing their applicability as pharmaceuticals, agrochemicals, or building blocks for organic materials. Despite the importance of this substituent, no general method exists for its installment onto functionalized aromatic

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