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线性分子式:
(C2H5O)3SiCH2Cl
化学文摘社编号:
分子量:
212.75
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
239-311-3
Beilstein/REAXYS Number:
1811785
MDL number:
InChI key
ZDOBWJOCPDIBRZ-UHFFFAOYSA-N
InChI
1S/C7H17ClO3Si/c1-4-9-12(7-8,10-5-2)11-6-3/h4-7H2,1-3H3
SMILES string
CCO[Si](CCl)(OCC)OCC
assay
96%
form
liquid
refractive index
n20/D 1.41 (lit.)
bp
173-176 °C (lit.)
density
1.022 g/mL at 25 °C (lit.)
Quality Level
General description
(Chloromethyl)triethoxysilane is an organotrialkoxy silane based reagent with chloromethyl as the organofunctional group. It can be used as a starting material for the synthesis of silane based polymers.
Application
发生相应的格氏自缩合,形成多官能碳硅烷。
Influence of the alkyl chain length of HSO3-R-MCM-41 on the esterification of glycerol with fatty acids
DIAZ I, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 80(1-3), 33-42 (2005)
Effect of spacer groups on the performance of MCM-41-supported platinum cluster-derived hydrogenation catalysts
Maity N, et al.
J. Catal., 242(2), 332-339 (2006)
Tetrahedron Letters, 34, 2111-2111 (1993)
Siloxane functionalized cyclopentadienyl-molybdenum complexes: Synthesis, characterization and catalytic application
Zhao J, et al.
Inorgorganica Chimica Acta, 358(14), 4201-4207 (2005)
Priyanka Reddy et al.
Scientific reports, 9(1), 9364-9364 (2019-06-30)
The neuroactive mycotoxin lolitrem B causes a neurological syndrome in grazing livestock resulting in hyperexcitability, muscle tremors, ataxia and, in severe cases, clonic seizures and death. To define the effects of the major toxin lolitrem B in the brain, a
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