108238-09-1 | 2-Phenoxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$7.00	$5.00
5g	98%	in stock	$31.00	$22.00
10g	95%	in stock	$31.00	$22.00
25g	95%	in stock	$77.00	$54.00

Description

• Catalog Number: AD78074
• Chemical Name: 2-Phenoxyphenylboronic acid
• CAS Number: 108238-09-1
• Molecular Formula: C12H11BO3
• Molecular Weight: 214.0249
• MDL Number: MFCD01001592
• SMILES: OB(c1ccccc1Oc1ccccc1)O

Computed Properties

• Complexity: 204
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

2-Phenoxybenzeneboronic acid is a versatile compound used in various chemical synthesis processes, primarily in the field of organic chemistry. This compound serves as a key building block in the preparation of numerous pharmaceuticals, agrochemicals, and advanced materials.One of the prominent applications of 2-Phenoxybenzeneboronic acid is in Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl halide with an arylboronic acid in the presence of a palladium catalyst to form a new carbon-carbon bond. 2-Phenoxybenzeneboronic acid, being an arylboronic acid, can participate in this reaction, allowing for the synthesis of biaryl compounds which are commonly found in pharmaceuticals and materials science.Furthermore, 2-Phenoxybenzeneboronic acid can also be utilized in the synthesis of polymer materials, where its boronic acid functionality can act as a key binding site for crosslinking reactions. This property enables the incorporation of 2-Phenoxybenzeneboronic acid into polymers, enhancing their properties and expanding their applications in fields such as coatings and adhesives.Overall, the application of 2-Phenoxybenzeneboronic acid in chemical synthesis showcases its significance as a valuable reagent in the preparation of complex and functional organic molecules with diverse applications across industries.