1119899-37-4 | 7-Cyanobenzo[b]thiophen-2-ylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	90%	in stock	$462.00	$323.00
1g	90%	in stock	$477.00	$334.00
5g	90%	in stock	$1,624.00	$1,137.00
10g	90%	in stock	$2,498.00	$1,749.00

Description

• Catalog Number: AE11768
• Chemical Name: 7-Cyanobenzo[b]thiophen-2-ylboronic acid
• CAS Number: 1119899-37-4
• Molecular Formula: C9H6BNO2S
• Molecular Weight: 203.0254
• MDL Number: MFCD16877453
• SMILES: N#Cc1cccc2c1sc(c2)B(O)O

Upstream Synthesis Route

(7-Cyanobenzo[b]thiophen-2-yl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in various organic transformations. Its unique structure containing a boronic acid moiety attached to a thiophene ring offers a range of reactivity and selectivity in synthetic reactions.This compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it serves as a boronate ester partner to form carbon-carbon bonds with aryl halides or aryl triflates. The boronic acid functionality allows for mild reaction conditions and high yields, making it a preferred reagent in the synthesis of biaryl compounds, pharmaceuticals, agrochemicals, and functional materials.Additionally, (7-Cyanobenzo[b]thiophen-2-yl)boronic acid can participate in diverse transformations such as C-H activation, nucleophilic addition, and transition metal-catalyzed coupling reactions. Its versatile nature and compatibility with various functional groups make it a valuable tool for organic chemists seeking to construct complex molecular structures efficiently and selectively.Overall, the application of (7-Cyanobenzo[b]thiophen-2-yl)boronic acid in chemical synthesis demonstrates its significance as a key component in modern organic chemistry, enabling the development of novel molecules with diverse applications across industries.