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Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane

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Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane Basic information

Product Name:
Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane
Synonyms:
  • ((Epoxycyclohexyl)ethyl)trimethoxy silane
  • (3,4-epoxycyclohexyl)ethyltrimethoxysilane
  • 2-(3,4-Epoxycyclohexyl) ethyltriacetoxysilane
  • 3,4-Epoxycyclohexylethyltrimethoxysilane
  • 3-[2-(Trimethoxysilyl)Ethyl]-7-oxabicyclo[4.1.0]heptane
  • 4-[2-(Trimethoxysilyl)ethyl]-7-oxabicyclo[4.1.0]heptane
  • A 186
  • A 186 (Heterocycle)
CAS:
3388-04-3
MF:
C11H22O4Si
MW:
246.38
EINECS:
222-217-1
Product Categories:
  • Industrial/Fine Chemicals
  • Epoxy Silanes (Silane Coupling Agents)
  • Functional Materials
  • Si (Classes of Silicon Compounds)
  • Silane Coupling Agents
  • Si-O Compounds
  • Trialkoxysilanes
  • silane
Mol File:
3388-04-3.mol
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Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane Chemical Properties

Melting point:
<0°C
Boiling point:
310 °C(lit.)
Density 
1.065 g/mL at 25 °C(lit.)
vapor pressure 
0.46Pa at 25℃
refractive index 
n20/D 1.451(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
liquid
Specific Gravity
1.065
color 
Colorless to Almost colorless
Water Solubility 
1.4g/L at 20℃
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
8980119
InChIKey
DQZNLOXENNXVAD-UHFFFAOYSA-N
LogP
2.5 at 20℃
CAS DataBase Reference
3388-04-3(CAS DataBase Reference)
NIST Chemistry Reference
1-[2-(Trimethoxysilyl)ethyl]cyclohexane-3,4-epoxide(3388-04-3)
EPA Substance Registry System
3,4-Epoxycyclohexylethyltrimethoxysilane (3388-04-3)
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Safety Information

Hazard Codes 
T
Risk Statements 
45-46-45/46
Safety Statements 
53-23-36/37/39-45
WGK Germany 
3
RTECS 
VV4000000
3-10
TSCA 
Yes
HS Code 
29319090
Toxicity
LD50 oral in rat: 8mL/kg

MSDS

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Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane Usage And Synthesis

Uses

Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane may be used as a precursor to form SiCOH film via sol-gel. The silane may be used to functionalize alumina nanoparticles towards the fabrication of polyamide 12/alumina nanocomposites. 4 Basalt fibers were functionalized with this silane and its consequent effect on the fabrication of basalt fiber–epoxidized vegetable oil matrix composite materials was analyzed.Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane can be used as a silane based coupling agent to functionalize a variety of substrates. It modifies the surface to improve the dispersion of nanoparticles. It can be used as an adhesion promoter by treating the precursor material with epoxy silanes.

Uses

Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane was used as an adhesion promoter during the fabrication of:

  • a photoacid generator activated by two photon excitation.
  • nanoscale polymeric structures (width: 65 nm) using 520 nm femtosecond pulse excitation.

Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane may be used as a precursor to form SiCOH film via sol-gel. The silane may be used to functionalize alumina nanoparticles towards the fabrication of polyamide 12/alumina nanocomposites. 4 Basalt fibers were functionalized with this silane and its consequent effect on the fabrication of basalt fiber–epoxidized vegetable oil matrix composite materials was analyzed.

Application

Trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane was used as an adhesion promoter during the fabrication of:a photoacid generator activated by two photon excitation.nanoscale polymeric structures (width: 65 nm) using 520 nm femtosecond pulse excitation.

Flammability and Explosibility

Non flammable

Synthesis


The apparatus of Example B was charged with 148.8 g (1.2 mol) of 1-vinyl-3,4-epoxycyclohexane, 1.3 g of a carboxylic acid promoter, and 0.15 ml of 10% chloroplatinic acid catalyst solution. The flask contents were heated to 89?? C. and dropwise addition of 122.8 g {[1.0 mol) of trimethoxysilane was begun. The reaction temperature was controlled at 90??-95?? C. with an ice bath. Reaction was maintained at that temperature for half an hour after completion of addition, which took 18 minutes. Analysis by gas chromatography showed a yield of 90% of 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane. This example demonstrates a standard preparation of 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane using commercial chloroplatinic acid.

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