所有图片(1)
About This Item
线性分子式:
ClC6H4Si(OC2H5)3
CAS号:
分子量:
274.82
EC 号:
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
方案
97%
折射率
n20/D 1.474 (lit.)
沸点
82-84 °C/0.07 mmHg (lit.)
密度
1.069 g/mL at 25 °C (lit.)
官能团
chloro
SMILES字符串
CCO[Si](OCC)(OCC)c1ccc(Cl)cc1
InChI
1S/C12H19ClO3Si/c1-4-14-17(15-5-2,16-6-3)12-9-7-11(13)8-10-12/h7-10H,4-6H2,1-3H3
InChI key
AFILDYMJSTXBAR-UHFFFAOYSA-N
应用
(4-Chlorophenyl)triethoxysilane can be used:
- To facilitate the connection between dipolar mixed monolayers and zinc oxide in photovoltaic devices.
- As a substrate in the Ni-catalyzed decarboxylative coupling with alkynyl carboxylic acids to yield substituted diarylalkynes.
- As a substrate in the Hiyama cross-coupling reactions with 3-iodoazetidines to yield substituted 3-arylazetidines.
- As an intermediate in the synthesis of tripod-shaped oligo(p-phenylene)s, which are used in the surface immobilization of gold and CdS quantum dots for sensor applications.
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
>230.0 °F - closed cup
闪点(°C)
> 110 °C - closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Palladium-Catalyzed Hiyama Cross-Couplings of Arylsilanes with 3-Iodoazetidine: Synthesis of 3-Arylazetidines
Liu Z, et al.
The Journal of Organic Chemistry, 84(19), 12358-12365 (2019)
Synthesis of azobenzene substituted tripod-shaped bi (p-phenylene) s. Adsorption on gold and CdS quantum-dots surfaces
Hierrezuelo J, et al.
Tetrahedron, 69(16), 3465-3474 (2013)
Tuning zinc oxide/organic energy level alignment using mixed triethoxysilane monolayers
Brenner TM, et al.
Journal of Material Chemistry C, 1(37), 5935-5943 (2013)
Nickel-catalyzed Hiyama-type decarboxylative coupling of propiolic acids and organosilanes
Edwin Raja GC, et al.
The Journal of Organic Chemistry, 81(12), 5244-5249 (2016)
Denmark, S. E.; Ober, M. H.
Aldrichimica Acta, 36, 75-75 (2003)
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