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1-PHENYL-1-TRIMETHYLSILOXYETHYLENE

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1-PHENYL-1-TRIMETHYLSILOXYETHYLENE Basic information

Product Name:
1-PHENYL-1-TRIMETHYLSILOXYETHYLENE
Synonyms:
  • 1-(Trimethylsilyloxy)-1-phenylethene
  • 1-Phenyl-1-trimethylsiloxyethene
  • 1-Phenylvinyl trimethylsilyl ether
  • (1-Phenylethenyloxy)trimethylsilane
  • [(1-Phenylethenyl)oxy]trimethylsilane
  • à-(trimethylsiloxy)styrene
  • α-(trimethylsiloxy)styrene
  • 1-PHENYL-1-TRIMETHYLSILOXYETHYLENE 97%
CAS:
13735-81-4
MF:
C11H16OSi
MW:
192.33
EINECS:
237-308-1
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Monoalkoxysilanes
  • Enol Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Si (Classes of Silicon Compounds)
  • Silicon Compounds (for Synthesis)
  • Si-O Compounds
  • Synthetic Organic Chemistry
Mol File:
13735-81-4.mol
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1-PHENYL-1-TRIMETHYLSILOXYETHYLENE Chemical Properties

Melting point:
122-123 °C
Boiling point:
88-89 °C/11 mmHg (lit.)
Density 
0.938 g/mL at 25 °C (lit.)
vapor density 
>1 (vs air)
refractive index 
n20/D 1.502(lit.)
Flash point:
174 °F
storage temp. 
2-8°C
form 
clear liquid
color 
Colorless to Light orange to Yellow
Specific Gravity
0.938
Water Solubility 
Reacts with water.
Sensitive 
Moisture Sensitive
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
1306914
CAS DataBase Reference
13735-81-4(CAS DataBase Reference)
EPA Substance Registry System
Silane, trimethyl[(1-phenylethenyl)oxy]- (13735-81-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-21
TSCA 
No
HS Code 
2931900090

MSDS

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1-PHENYL-1-TRIMETHYLSILOXYETHYLENE Usage And Synthesis

Uses

1-Phenyl-1-trimethylsiloxyethylene has been used in the synthesis of β-amino ketones in water via Mannich-type reaction and cis-2,6-disubstituted dihydropyrans via three-component, one-pot cascade reaction. It is also used as chemical additives and intermediates.

Uses

1-Phenyl-1-trimethylsiloxyethylene has been used in the synthesis of:

  • β-amino ketones in water via Mannich-type reaction
  • cis-2,6-disubstituted dihydropyrans via three-component, one-pot cascade reaction

General Description

1-Phenyl-1-trimethylsiloxyethylene is a styrene type silyl enol ether, reacts with formaldehyde and 2,4-pentanedione to yield the corresponding dihydropyran. It also undergoes Mukaiyama aldol reaction with aldehydes in water in the presence of amphiphilic calix[6]arene derivatives as surfactants.

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