2-Methyl-1-(Trimethylsiloxy)-1-Propene

95%

Reagent Code: #88205
fingerprint
CAS Number 6651-34-9

science Other reagents with same CAS 6651-34-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.29 g/mol
Formula C₇H₁₆OSi
badge Registry Numbers
MDL Number MFCD00192331
thermostat Physical Properties
Boiling Point 114-116°C 650mm Hg (Lit.)
inventory_2 Storage & Handling
Storage 2~8℃,Seal

description Product Description

This silyl enol ether is primarily employed as a reagent in organic synthesis, particularly in the Mukaiyama aldol reaction, where it serves as an enolate equivalent for stereoselective carbon-carbon bond formation. It is valuable for introducing protected enol functionalities and protecting carbonyl groups during multi-step syntheses of pharmaceuticals, fine chemicals, and agrochemicals. Its reactivity facilitates the construction of complex molecular architectures, making it essential in advanced organic transformations.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless Liquid
Purity 94.5-100
Refractive Index n20D 1.406-1.412

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,900.00
inventory 5g
10-20 days ฿7,900.00
inventory 25g
10-20 days ฿31,600.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Methyl-1-(Trimethylsiloxy)-1-Propene
No image available

This silyl enol ether is primarily employed as a reagent in organic synthesis, particularly in the Mukaiyama aldol reaction, where it serves as an enolate equivalent for stereoselective carbon-carbon bond formation. It is valuable for introducing protected enol functionalities and protecting carbonyl groups during multi-step syntheses of pharmaceuticals, fine chemicals, and agrochemicals. Its reactivity facilitates the construction of complex molecular architectures, making it essential in advanced organ

This silyl enol ether is primarily employed as a reagent in organic synthesis, particularly in the Mukaiyama aldol reaction, where it serves as an enolate equivalent for stereoselective carbon-carbon bond formation. It is valuable for introducing protected enol functionalities and protecting carbonyl groups during multi-step syntheses of pharmaceuticals, fine chemicals, and agrochemicals. Its reactivity facilitates the construction of complex molecular architectures, making it essential in advanced organic transformations.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...