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:
产品名称
苯基二甲基乙氧基硅, ≥97.0% (GC)
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.)
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.
General description
Ethoxydimethylphenylsilane undergoes trifluoroethanolysis in the presence of substituted acetic acids.{69}
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
The general acid catalyzed trifluoroethanolysis of ethoxydimethylphenylsilane
Dietze PE, et al.
Tetrahedron Letters, 32(3), 307-310 (1991)
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 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)
Synthesis of aggregation-resistant MFI nanoparticles
Chen H, et al.
Catalysis Today (2019)
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