1072952-43-2 | 5-Hydroxy-2-methoxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$86.00	$60.00
250mg	98%	in stock	$209.00	$147.00
1g	98%	in stock	$385.00	$269.00
5g	98%	in stock	$1,365.00	$955.00

Description

• Catalog Number: AB70816
• Chemical Name: 5-Hydroxy-2-methoxyphenylboronic acid
• CAS Number: 1072952-43-2
• Molecular Formula: C7H9BO4
• Molecular Weight: 167.95496
• MDL Number: MFCD07368831
• SMILES: COc1ccc(cc1B(O)O)O

Computed Properties

• Complexity: 141
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

5-Hydroxy-2-methoxyphenylboronic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. It serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and organic materials.One of the primary applications of $name$ is its role as a key reagent in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method enables the formation of carbon-carbon bonds, allowing chemists to efficiently connect different organic molecules together. By utilizing 5-Hydroxy-2-methoxyphenylboronic acid in these reactions, researchers can access a diverse array of complex structures with high efficiency and selectivity.Furthermore, $name$ is instrumental in the synthesis of biologically active compounds, such as pharmaceutical ingredients and natural product derivatives. Its unique reactivity and compatibility with a wide range of functional groups make it an indispensable tool for chemists working in medicinal chemistry and drug discovery.In addition to its role in carbon-carbon bond formation, 5-Hydroxy-2-methoxyphenylboronic acid also finds application in the functionalization of aromatic systems and the construction of heterocyclic compounds. Its versatility and ease of handling make it a valuable component in the toolbox of synthetic chemists seeking to explore new pathways and strategies in organic synthesis.