419982
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/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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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.
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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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