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419982

Sigma-Aldrich

Triethyl(trifluoromethyl)silane

98%

Synonym(s):

(Trifluoromethyl)triethylsilane, Triethylsilyl trifluoromethane

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About This Item

Linear Formula:
(C2H5)3SiCF3
CAS Number:
Molecular Weight:
184.27
Beilstein:
4242161
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

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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This Item
488712367265376264
reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

-

reaction suitability

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

refractive index

n20/D 1.382 (lit.)

refractive index

-

refractive index

n20/D 1.488 (lit.)

refractive index

n20/D 1.413 (lit.)

form

liquid

form

-

form

liquid

form

liquid

bp

56-57 °C/60 mmHg (lit.)

bp

54-55 °C (lit.)

bp

102-103 °C/0.5 mmHg (lit.)

bp

91-93 °C (lit.)

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

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

32.0 °F - closed cup

Flash Point(C)

0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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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