1025719-11-2 | 2-(4-Bromofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$325.00	$228.00
1g	98%	in stock	$791.00	$554.00
5g	98%	in stock	$2,345.00	$1,642.00
25g	98%	in stock	$5,454.00	$3,818.00

Description

• Catalog Number: AA09891
• Chemical Name: 2-(4-Bromofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS Number: 1025719-11-2
• Molecular Formula: C10H14BBrO3
• Molecular Weight: 272.9314
• MDL Number: MFCD12405449
• SMILES: CC1(C)OB(OC1(C)C)c1occ(c1)Br

Computed Properties

• Complexity: 241
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

2-(4-Bromofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound widely employed in chemical synthesis as a building block for constructing various organic molecules. Its unique structure combines the properties of a furan ring and a boronic ester, making it valuable for different synthetic applications.One key application of this compound is in the field of Suzuki coupling reactions. Suzuki coupling is a powerful method for forming carbon-carbon bonds and is often used in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. By incorporating 2-(4-Bromofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane as a boronic ester partner in a Suzuki coupling reaction, chemists can selectively and efficiently create new carbon-carbon bonds under mild reaction conditions.Additionally, this compound is utilized in the preparation of functionalized organoboron compounds, which serve as vital intermediates in organic synthesis. The unique reactivity of the boronic ester group allows for further functionalization of the molecule, enabling the introduction of diverse functional groups into the final product.Overall, 2-(4-Bromofuran-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane plays a crucial role in enabling the synthesis of complex organic molecules through Suzuki coupling reactions and the preparation of functionalized organoboron compounds. Its versatility and reactivity make it a valuable tool for chemists engaged in the development of novel compounds with various applications.