1048330-10-4 | 3-(Methoxycarbonyl)-4-methylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$10.00	$7.00
250mg	98%	in stock	$20.00	$14.00
1g	98%	in stock	$54.00	$38.00

Description

• Catalog Number: AD69597
• Chemical Name: 3-(Methoxycarbonyl)-4-methylphenylboronic acid
• CAS Number: 1048330-10-4
• Molecular Formula: C9H11BO4
• Molecular Weight: 193.9922
• MDL Number: MFCD13191800
• SMILES: COC(=O)c1cc(ccc1C)B(O)O

Computed Properties

• Complexity: 207
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

(3-(Methoxycarbonyl)-4-methylphenyl)boronic acid, also known as $name$, is a versatile compound that finds wide application in chemical synthesis. As a boronic acid derivative, $name$ serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, (3-(Methoxycarbonyl)-4-methylphenyl)boronic acid acts as a valuable reagent in Suzuki-Miyaura cross-coupling reactions. This important reaction allows for the formation of carbon-carbon bonds under mild conditions, enabling the synthesis of complex organic molecules. By serving as a coupling partner in this reaction, $name$ facilitates the construction of biaryl compounds and other structurally diverse products.Furthermore, (3-(Methoxycarbonyl)-4-methylphenyl)boronic acid is often utilized in the preparation of functionalized building blocks for organic synthesis. Its unique boronic acid functionality enables it to participate in diverse transformations, such as metal-catalyzed cross-coupling reactions and carbon-carbon bond formations. This flexibility and reactivity make $name$ an indispensable tool for chemists engaged in the synthesis of intricate organic molecules.Overall, the application of (3-(Methoxycarbonyl)-4-methylphenyl)boronic acid in chemical synthesis underscores its significance as a key reagent for the construction of complex molecules in various research and industrial settings.