31469-15-5 | Dimethylketene methyl trimethylsilyl acetal

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$19.00	$13.00
5g	97%	in stock	$28.00	$19.00
10g	97%	in stock	$45.00	$31.00
25g	97%	in stock	$76.00	$53.00

Description

• Catalog Number: AB45943
• Chemical Name: Dimethylketene methyl trimethylsilyl acetal
• CAS Number: 31469-15-5
• Molecular Formula: C8H18O2Si
• Molecular Weight: 174.3128
• MDL Number: MFCD00010232
• SMILES: COC(=C(C)C)O[Si](C)(C)C

Computed Properties

• Complexity: 152
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

1-Methoxy-2-methyl-1-(trimethylsiloxy)propene, also known as $name$, is a versatile compound widely used in various chemical synthesis processes. This compound serves as a valuable building block in organic synthesis due to its unique chemical properties.One major application of $name$ in chemical synthesis is as a key intermediate in the preparation of organosilicon compounds. By utilizing $name$ as a starting material, chemists can easily introduce functional groups such as methoxy and trimethylsiloxy groups into the target molecules, enabling the modification and enhancement of their properties.Furthermore, $name$ can be utilized in the synthesis of complex organic molecules, particularly in the formation of heterocycles and pharmaceutical intermediates. Its ability to undergo various chemical transformations, such as nucleophilic additions and eliminations, makes it a valuable tool for creating diverse chemical structures with desired functionalities.In addition, $name$ finds applications in the preparation of advanced materials, including polymers, resins, and surfactants. Its incorporation into polymer chains can impart specific characteristics such as improved thermal stability, flexibility, and resistance to oxidation.Overall, the versatility of 1-Methoxy-2-methyl-1-(trimethylsiloxy)propene makes it an essential component in the toolkit of synthetic chemists, enabling the efficient and precise construction of complex organic molecules and materials for various industrial and scientific applications.

Literature

• P(PhCH2NCH2CH2)3N catalysis of Mukaiyama aldol reactions of aliphatic, aromatic, and heterocyclic aldehydes and trifluoromethyl phenyl ketone.

  The Journal of organic chemistry 20091106

• Amphiphilic model conetworks based on cross-linked star copolymers of benzyl methacrylate and 2-(dimethylamino)ethyl methacrylate: synthesis, characterization, and DNA adsorption studies.

  Biomacromolecules 20061201