41409
苯基二甲基乙氧基硅
≥97.0% (GC)
别名:
二甲基乙氧基苯基硅烷, 二甲基苯基乙氧基硅烷
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关于此项目
经验公式（希尔记法）:
C10H16OSi
化学文摘社编号:
分子量:
180.32
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-366-4
Beilstein/REAXYS Number:
2936696
MDL number:
InChI key
FIHCECZPYHVEJO-UHFFFAOYSA-N
InChI
1S/C10H16OSi/c1-4-11-12(2,3)10-8-6-5-7-9-10/h5-9H,4H2,1-3H3
SMILES string
CCO[Si](C)(C)c1ccccc1
assay
≥97.0% (GC)
refractive index
n20/D 1.479
bp
93 °C/25 mmHg (lit.)
density
0.924 g/mL at 20 °C (lit.)
General description
Ethoxydimethylphenylsilane undergoes trifluoroethanolysis in the presence of substituted acetic acids.{69}
Application
Ethoxydimethylphenylsilane can be used:
- To functionalize SiO2 nanoparticles by the sol-gel method used in the bilayer coatings on a glass surface.
- To functionalize the nanosized zeolites applicable in the catalysis.
- As a substrate in the study of Si-O bond cleavage in the presence of serine hydrolases.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Synthesis of aggregation-resistant MFI nanoparticles
Chen H, et al.
Catalysis Today (2019)
The influence of new hydrophobic silica nanoparticles on the surface properties of the films obtained from bilayer hybrids
Petcu C, et al.
Nanomaterials, 7(2), 47-47 (2017)
On the biocatalytic cleavage of silicon--oxygen bonds: A substrate structural approach to investigating the cleavage of protecting group silyl ethers by serine-triad hydrolases
Maraite A, et al.
Journal of Molecular Catalysis. B, Enzymatic, 56(1), 24-28 (2009)
The general acid catalyzed trifluoroethanolysis of ethoxydimethylphenylsilane
Dietze PE, et al.
Tetrahedron Letters, 32(3), 307-310 (1991)
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