1126-93-8 | 2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$25.00	$17.00
5g	95%	in stock	$58.00	$41.00
25g	95%	in stock	$174.00	$122.00

Description

• Catalog Number: AD75541
• Chemical Name: 2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS Number: 1126-93-8
• Molecular Formula: C8H17BO3
• Molecular Weight: 172.02977999999996
• MDL Number: MFCD22054335
• SMILES: CCOB1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 152
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in organic chemistry, particularly in the field of cross-coupling reactions and carbon-carbon bond formation.One of the key applications of 2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is its role as a boron reagent in Suzuki-Miyaura cross-coupling reactions. In this process, $name$ functions as a boronic ester source, which reacts with an organic halide in the presence of a palladium catalyst to form a new carbon-carbon bond. This method is widely used in pharmaceutical, agrochemical, and material science research to synthesize complex organic molecules efficiently.Additionally, 2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is also utilized in the construction of biologically active compounds, natural product synthesis, and the development of new materials. Its unique structure and reactivity make it a valuable reagent for organic chemists seeking to streamline their synthetic routes and access a diverse array of chemical compounds.In summary, 2-Ethoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane plays a crucial role in modern chemical synthesis by enabling the efficient construction of complex organic molecules through cross-coupling reactions and carbon-carbon bond formation. Its versatility and utility make it an indispensable tool for researchers and chemists in various fields of organic chemistry.