1027045-31-3 | 2,6-Dimethyl-4-chlorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$73.00	$51.00
250mg	95%	in stock	$95.00	$66.00
1g	95%	in stock	$205.00	$143.00
5g	95%	in stock	$643.00	$450.00
25g	95%	in stock	$2,314.00	$1,620.00

Description

• Catalog Number: AA10382
• Chemical Name: 2,6-Dimethyl-4-chlorophenylboronic acid
• CAS Number: 1027045-31-3
• Molecular Formula: C8H10BClO2
• Molecular Weight: 184.4278
• MDL Number: MFCD10566594
• SMILES: OB(c1c(C)cc(cc1C)Cl)O

Computed Properties

• Complexity: 142
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

The (4-Chloro-2,6-dimethylphenyl)boronic acid is a valuable building block in organic synthesis due to its unique reactivity. This compound is commonly utilized in the formation of carbon-carbon and carbon-heteroatom bonds, making it a versatile tool for chemists in various fields.One of the key applications of (4-Chloro-2,6-dimethylphenyl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. This palladium-catalyzed reaction enables the formation of biaryl compounds by coupling an aryl halide with an arylboronic acid derivative. The (4-Chloro-2,6-dimethylphenyl)boronic acid serves as an important arylboronic acid component in this reaction, allowing for the synthesis of a wide range of pharmaceuticals, agrochemicals, and materials.Additionally, (4-Chloro-2,6-dimethylphenyl)boronic acid can be employed in the construction of complex organic molecules through other transformations such as Buchwald-Hartwig amination, Chan-Lam coupling, and Stille coupling reactions. Its ability to undergo these diverse reactions highlights its significance in modern organic synthesis for the creation of novel compounds and materials.