100045-83-8 | Stannane, tributyl[(methoxymethoxy)methyl]-

Packsize	Purity	Availability	Price	Discounted Price
1g	94%	in stock	$372.00	$260.00
5g	94%	in stock	$1,443.00	$1,010.00

Description

• Catalog Number: AA00657
• Chemical Name: Stannane, tributyl[(methoxymethoxy)methyl]-
• CAS Number: 100045-83-8
• Molecular Formula: C15H34O2Sn
• Molecular Weight: 365.1303
• MDL Number: MFCD03412101
• SMILES: CCCC[Sn](CCCC)(CCCC)COCOC

Upstream Synthesis Route

Tributyl((methoxymethoxy)methyl)stannane, commonly referred to as TBMMST, is a versatile organotin compound widely utilized in chemical synthesis. Renowned for its unique reactivity and alkylating properties, TBMMST plays a crucial role in various synthetic processes, particularly in the field of organic chemistry.One of the key applications of TBMMST in chemical synthesis is as a reliable source of alkyl radicals. By serving as a radical precursor, TBMMST facilitates radical-mediated reactions such as radical additions, substitutions, and polymerizations. Its ability to generate alkyl radicals under mild conditions makes it a valuable tool in the construction of complex organic molecules and polymers.TBMMST also finds extensive use in the synthesis of organotin compounds through Stille coupling reactions. In this process, TBMMST acts as an alkylating agent, forming carbon-carbon bonds with organic halides or pseudohalides under palladium catalysis. The versatility of TBMMST in Stille couplings enables the efficient synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and materials.Furthermore, TBMMST is employed in the synthesis of functional materials, where its alkyl moiety serves as a reactive handle for further derivatization. By strategically incorporating TBMMST into molecular structures, chemists can introduce specific functionalities or modify material properties, leading to the development of advanced materials with tailored characteristics.Overall, Tributyl((methoxymethoxy)methyl)stannane emerges as a valuable reagent in chemical synthesis, offering precise alkyl radical generation, efficient carbon-carbon bond formation, and versatile functionalization capabilities for the synthesis of diverse organic compounds and materials.