55499-44-0 | 2,4-Dimethylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$7.00	$5.00
5g	98%	in stock	$16.00	$11.00
10g	98%	in stock	$28.00	$19.00
25g	98%	in stock	$61.00	$43.00
100g	98%	in stock	$188.00	$132.00

Description

• Catalog Number: AB60311
• Chemical Name: 2,4-Dimethylphenylboronic acid
• CAS Number: 55499-44-0
• Molecular Formula: C8H11BO2
• Molecular Weight: 149.9827
• MDL Number: MFCD02683101
• SMILES: Cc1ccc(c(c1)C)B(O)O

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

2,4-Dimethylbenzeneboronic acid, also known as p-xyleneboronic acid, is a valuable building block and reagent in chemical synthesis. This compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, which are widely used in organic synthesis to form carbon-carbon bonds. By participating in this reaction, 2,4-dimethylbenzeneboronic acid facilitates the coupling of aryl halides or pseudohalides with aryl or alkenyl boronic acids, leading to the formation of various biaryl compounds.Moreover, 2,4-dimethylbenzeneboronic acid can also be employed in the preparation of pharmaceuticals, agrochemicals, and materials. Its versatile nature allows for the functionalization of aromatic compounds, enabling the introduction of specific substituents for the synthesis of target molecules. Additionally, the boronic acid moiety in this compound can undergo further transformations, such as oxidation to the corresponding phenol or reduction to the corresponding alcohol, expanding its synthetic utility.In summary, 2,4-Dimethylbenzeneboronic acid serves as a valuable tool in organic synthesis, enabling the formation of complex molecular structures through Suzuki-Miyaura cross-coupling reactions and other transformations. Its broad applications make it a crucial reagent in the toolkit of synthetic chemists for the preparation of diverse chemical compounds.