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
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4242161
Assay:
98%
Form:
liquid
InChI
1S/C7H15F3Si/c1-4-11(5-2,6-3)7(8,9)10/h4-6H2,1-3H3
SMILES string
CC[Si](CC)(CC)C(F)(F)F
InChI key
ZHSKFONQCREGOG-UHFFFAOYSA-N
assay
98%
form
liquid
reaction suitability
reaction type: C-C Bond Formation
Quality Level
bp
56-57 °C/60 mmHg (lit.)
density
0.98 g/mL at 25 °C (lit.)
functional group
fluoro
Related Categories
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.
signalword
Danger
hcodes
pcodes
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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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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