419982
三乙基(三氟甲基)硅烷
98%
别名:
(三氟甲基)三乙基硅烷, 三乙基甲硅烷基三氟甲烷
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关于此项目
线性分子式:
(C2H5)3SiCF3
化学文摘社编号:
分子量:
184.27
Beilstein:
4242161
MDL编号:
UNSPSC代码:
12352001
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
98%
表单
liquid
反应适用性
reaction type: C-C Bond Formation
折射率
n20/D 1.382 (lit.)
沸点
56-57 °C/60 mmHg (lit.)
密度
0.98 g/mL at 25 °C (lit.)
官能团
fluoro
SMILES字符串
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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应用
Reactant for:
- Trifluoromethylation of aryl iodides
- Trialkylsilylation reactions
- Used for deposition of perfluoro-methyl silica films
包装
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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