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Dimethoxymethylphenylsilane

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Dimethoxymethylphenylsilane Basic information

Product Name:
Dimethoxymethylphenylsilane
Synonyms:
  • METHYLPHENYLDIMETHOXYSILANE
  • dimethoxymethylphenyl-silan
  • Dimethoxyphenylmethylsilane
  • Fenyl-dimethoxy-methylsilan
  • PHENYLMETHYLDIMETHOXYSILANE
  • DIMETHOXYMETHYLPHENYLSILANE
  • Z 6073
  • Methylphenyldimethoxysylane
CAS:
3027-21-2
MF:
C9H14O2Si
MW:
182.29
EINECS:
221-192-4
Product Categories:
  • organosilicon compounds
  • Organics
  • Dialkoxysilanes
  • Functional Materials
  • Si (Classes of Silicon Compounds)
  • Silane Coupling Agents
  • Silane Coupling Agents (Intermediates)
  • Si-O Compounds
  • Phenyl Silanes
  • 3027-21-2
Mol File:
3027-21-2.mol
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Dimethoxymethylphenylsilane Chemical Properties

Melting point:
73-75 °C
Boiling point:
199 °C(lit.)
Density 
1.005 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.479
Flash point:
80 °C
storage temp. 
Inert atmosphere,Room Temperature
form 
liquid
Specific Gravity
0.993
color 
colorless
Sensitive 
moisture sensitive
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
InChIKey
CVQVSVBUMVSJES-UHFFFAOYSA-N
CAS DataBase Reference
3027-21-2(CAS DataBase Reference)
NIST Chemistry Reference
Silane, dimethoxymethylphenyl-(3027-21-2)
EPA Substance Registry System
Dimethoxymethylphenylsilane (3027-21-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
VV3645000
10-21
TSCA 
Yes
HS Code 
29319090
Toxicity
mouse,LD50,oral,680mg/kg (680mg/kg),"Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 1234, 1986.

MSDS

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Dimethoxymethylphenylsilane Usage And Synthesis

Chemical Properties

Colorless or yellowish transparent liquid

Uses

The reaction of dimethoxymethylphenylsilane with Li metal in excess Me3SiCl in THF to produce the products the diastereomeric isomers of 2-[2,2-bis(trimethylsilyl)ethylidene]-1-methoxy-1-methyl-3,4,5-tris(trimethylsilyl)silolane, contracted from six- to five-membered rings, as well as the expected products dimethoxymethyl(Ttc)silane synthesized via a Birch-type reductive silylation[1].

Synthesis

Sodium metal particles suspension was added to a mixture of 62.5 g of chlorobenzene and 227 g of methyltrimethoxysilane, and then 0.32 g of 15-crown-5 was added. The reaction was carried out at 38 ° C for 2 h , The reaction was stopped, and the reaction mixture was filtered and vacuum-distilled to give Dimethoxymethylphenylsilane in a yield of 87%.

References

[1] Young Mook Lim, & Myong Euy Lee*. “An Unexpected Ring Contraction: Phenylsilane to Silacyclopentane.” Organometallics 27 5 (2008): 1000–1004.

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