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419982

Triethyl(trifluoromethyl)silane

Name: Triethyl(trifluoromethyl)silane
Brand: ALDRICH

98%

Synonym(s):

(Trifluoromethyl)triethylsilane, Triethylsilyl trifluoromethane

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About This Item

Linear Formula:

(C₂H₅)₃SiCF₃

CAS Number:

120120-26-5

Molecular Weight:

184.27

UNSPSC Code:

12352001

NACRES:

NA.22

PubChem Substance ID:

24866298

MDL number:

MFCD00192520

Beilstein/REAXYS Number:

4242161

Assay:

98%

Form:

liquid

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Quality Level

200

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

Related Categories

C-C Bond Forming Reagents

Chemical Synthesis

Silanes

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.

pictograms

GHS02

signalword

Danger

hcodes

H225

pcodes

P210

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

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

Regulatory Information

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The palladium-catalyzed trifluoromethylation of aryl chlorides.

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

Global Trade Item Number

SKU	GTIN
419982-1G	04061832092843

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