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Allyltrimethoxysilane

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Allyltrimethoxysilane Basic information

Product Name:
Allyltrimethoxysilane
Synonyms:
  • Silane,trimethoxy-2-propenyl-
  • trimethoxy-2-propenyl-silan
  • trimethoxy-2-propenyl-Silane
  • TRIMETHOXYALLYLSILANE
  • Allyltrimethoxysilane, 97+%
  • 3-(Trimethoxysilyl)-1-propene
  • Allytrimethoxysilane
  • AllyltriMethoxysilane, 97+% 5ML
CAS:
2551-83-9
MF:
C6H14O3Si
MW:
162.26
EINECS:
219-855-8
Product Categories:
  • Solution Deposition Precursors
  • Functional Materials
  • Si (Classes of Silicon Compounds)
  • Silane Coupling Agents
  • Si-O Compounds
  • Trialkoxysilanes
  • Vinyl Silanes (Silane Coupling Agents)
  • Vinylsilanes, Allylsilanes
  • SilanesOrganometallic Reagents
  • Organosilicon
  • Self Assembly&Contact Printing
  • Self-Assembly Materials
Mol File:
2551-83-9.mol
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Allyltrimethoxysilane Chemical Properties

Boiling point:
146-148 °C (lit.)
Density 
0.963 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.405(lit.)
Flash point:
88 °F
storage temp. 
Inert atmosphere,2-8°C
form 
Liquid
color 
Clear colorless
Specific Gravity
0.96
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
2350745
InChIKey
LFRDHGNFBLIJIY-UHFFFAOYSA-N
EPA Substance Registry System
Silane, trimethoxy-2-propenyl- (2551-83-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
26-36-37/39-16
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
10-21
TSCA 
Yes
HazardClass 
3.1
PackingGroup 
II
HS Code 
29319090

MSDS

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Allyltrimethoxysilane Usage And Synthesis

Chemical Properties

Colorless to Almost colorless clear liquid to slightly cloudy liquid

Uses

Allyltrimethoxysilane is an allylating reagent that can be used for the allylation of carbonyl compounds such as aldehydes, ketones, and imines. Homoallylic alcohols and amines are obtained via the C-C bond forming reaction. It can also be used to synthesize homoallylic α-branched amines from aromatic and aliphatic aldehyde hydrazones, and ketone hydrazones.

Application

Allyltrimethoxysilane as the Reagent of Double Bond Introduction to Porous Silica for Preparation of a Chiral Stationary Phase in Comparison with Allyltriethoxysilane.
Allylation of ketones, aldehydes and imines with dual activation of a Lewis Acid and fluoride ion.
Used in the regioselective generation of the thermodynamically more stable enol trimethoxysilyl ethers, which in turn are used in the asymmetric generation of quaternary carbon centers.
Converts arylselenyl bromides to arylallylselenides.
Allylates aryl iodides.
Allyltrimethoxysilane serves as a remarkable reagent in Silver-Catalyzed Asymmetric Allylation.

AllyltrimethoxysilaneSupplier

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