CAS 59414-23-2 1-Methoxy-3-Trimethylsiloxy-1,3-Butadiene

Catalog Number	ACM59414232-2
CAS Number	59414-23-2
Structure
Molecular Weight	172.3 g/mol
Molecular Formula	C8H16O2Si
Application	1-Methoxy-3-Trimethylsiloxy-13-Butadiene serves as a versatile reagent in various synthetic applications It is primarily used in the Mannich-Michael reaction to produce piperidinones and enaminones Additionally it acts as a functionalized Diels-Alder diene in the formation of pyridones and pyranones This compound is also involved in the synthesis of sulfone analogues akin to griseofulvin known as sulfogriseofulvins as well as 4H-1-aminopyrroles and 45H-pyrazoles The compound also referred to as Danishefsky's diene has been explored in a Mukaiyama-Michael-type addition/heterocyclization with 12-diaza-13-butadiene and in asymmetric hetero-Diels-Alder cyclizations with benzaldehyde facilitated by mesoporous inorganic/metal-organic hybrid catalysts

Catalog Number

ACM59414232-2

CAS Number

59414-23-2

Structure

Molecular Weight

172.3 g/mol

Molecular Formula

C8H16O2Si

Application

1-Methoxy-3-Trimethylsiloxy-13-Butadiene serves as a versatile reagent in various synthetic applications It is primarily used in the Mannich-Michael reaction to produce piperidinones and enaminones Additionally it acts as a functionalized Diels-Alder diene in the formation of pyridones and pyranones This compound is also involved in the synthesis of sulfone analogues akin to griseofulvin known as sulfogriseofulvins as well as 4H-1-aminopyrroles and 45H-pyrazoles The compound also referred to as Danishefsky's diene has been explored in a Mukaiyama-Michael-type addition/heterocyclization with 12-diaza-13-butadiene and in asymmetric hetero-Diels-Alder cyclizations with benzaldehyde facilitated by mesoporous inorganic/metal-organic hybrid catalysts

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