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线性分子式:
(C2H5)3SiCF3
化学文摘社编号:
分子量:
184.27
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4242161
产品名称
三乙基(三氟甲基)硅烷, 98%
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
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
Quality Level
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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.
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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