All Photos(1)
Synonym(s):
(Trifluoromethyl)triethylsilane, Triethylsilyl trifluoromethane
Linear Formula:
(C2H5)3SiCF3
CAS Number:
Molecular Weight:
184.27
Beilstein:
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.)
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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Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
WGK
WGK 3
Flash Point(F)
32.0 °F
Flash Point(C)
0 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
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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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