1010097-71-8 | 2-Ethoxy-3-fluorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$30.00	$21.00
1g	97%	in stock	$64.00	$45.00
5g	97%	in stock	$249.00	$175.00
10g	97%	in stock	$401.00	$281.00
25g	97%	in stock	$616.00	$431.00
100g	97%	in stock	$1,878.00	$1,315.00

Description

• Catalog Number: AA04322
• Chemical Name: 2-Ethoxy-3-fluorophenylboronic acid
• CAS Number: 1010097-71-8
• Molecular Formula: C8H10BFO3
• Molecular Weight: 183.9726
• MDL Number: MFCD11520053
• SMILES: CCOc1c(F)cccc1B(O)O

Upstream Synthesis Route

The (2-Ethoxy-3-fluorophenyl)boronic acid is a versatile compound widely utilized in chemical synthesis as a valuable building block in organic reactions. This boronic acid derivative serves as a crucial reagent in the synthesis of pharmaceuticals, agrochemicals, and materials due to its unique molecular properties.In organic chemistry, (2-Ethoxy-3-fluorophenyl)boronic acid is commonly employed in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds efficiently. This reaction allows for the formation of complex molecular structures with high selectivity and yield. The boronic acid functionality enables the compound to undergo further transformations, such as oxidation or reduction, to introduce various functional groups into the target molecules.Furthermore, (2-Ethoxy-3-fluorophenyl)boronic acid can participate in transition metal-catalyzed reactions, including Heck and Negishi couplings, enabling the rapid and controlled synthesis of diverse organic compounds. Its compatibility with a wide range of substrates makes it a valuable tool in the development of novel chemical entities in drug discovery and materials science.Overall, the application of (2-Ethoxy-3-fluorophenyl)boronic acid in chemical synthesis offers a strategic approach to access structurally diverse compounds with potential applications in pharmaceutical, agricultural, and material science industries.