1001108-64-0 | 2-(Carboxymethyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$325.00	$228.00
1g	96%	in stock	$791.00	$554.00
5g	96%	in stock	$1,973.00	$1,381.00

Description

• Catalog Number: AA01059
• Chemical Name: 2-(Carboxymethyl)phenylboronic acid
• CAS Number: 1001108-64-0
• Molecular Formula: C8H9BO4
• Molecular Weight: 179.9657
• MDL Number: MFCD08704668
• SMILES: OC(=O)Cc1ccccc1B(O)O

Computed Properties

• Complexity: 183
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3

Upstream Synthesis Route

2-(2-Boronophenyl)acetic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique boron-containing structure. In chemical synthesis, 2-(2-Boronophenyl)acetic acid is utilized as a key reagent for the formation of carbon-carbon and carbon-nitrogen bonds. It is particularly valuable in the preparation of pharmaceuticals, agrochemicals, and materials science.For example, this compound can be employed in the Suzuki-Miyaura cross-coupling reaction, a fundamental synthetic method in organic chemistry. The boron group in 2-(2-Boronophenyl)acetic acid acts as a versatile handle for introducing functional groups and modifying the reactivity of the molecule. Furthermore, the presence of the boron atom enables further transformations through metal-catalyzed reactions, making it a valuable tool for the construction of complex molecular structures.Overall, the application of 2-(2-Boronophenyl)acetic acid in chemical synthesis showcases its remarkable versatility and importance in modern organic chemistry, contributing to the development of novel compounds with diverse functionalities.

Literature

• Palladium(II)-catalyzed annulation of alkynes with ortho-ester-containing phenylboronic acids.

  Organic letters 20071011