101251-09-6 | 4-Acetylaminophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$7.00	$5.00
1g	96%	in stock	$9.00	$6.00
5g	96%	in stock	$35.00	$25.00
10g	96%	in stock	$66.00	$46.00
25g	96%	in stock	$136.00	$95.00
100g	96%	in stock	$542.00	$379.00

Description

• Catalog Number: AA05038
• Chemical Name: 4-Acetylaminophenylboronic acid
• CAS Number: 101251-09-6
• Molecular Formula: C8H10BNO3
• Molecular Weight: 178.9809
• MDL Number: MFCD02179451
• SMILES: OB(c1ccc(cc1)NC(=O)C)O

Computed Properties

• Complexity: 178
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

4-Acetamidophenylboronic acid, also known as 4-Acetamidophenylboronic acid, is a versatile compound commonly used in chemical synthesis. This chemical is a key building block in organic chemistry and has a wide range of applications in various reactions and processes.One of the primary uses of 4-Acetamidophenylboronic acid is as a crucial reagent in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by a palladium catalyst, is widely utilized in organic synthesis to form carbon-carbon bonds between aryl halides or pseudohalides and boronic acids. In this context, 4-Acetamidophenylboronic acid acts as a nucleophilic partner in the cross-coupling reaction, facilitating the formation of complex organic molecules.Furthermore, 4-Acetamidophenylboronic acid can be employed in the synthesis of biologically active compounds, pharmaceuticals, agrochemicals, and materials. Its unique boronic acid functionality allows for selective reactions with electrophiles, enabling the introduction of functional groups at specific positions in organic molecules. This flexibility makes 4-Acetamidophenylboronic acid a valuable tool for chemists in designing and constructing structurally diverse and complex organic compounds.Overall, the application of 4-Acetamidophenylboronic acid in chemical synthesis extends to various fields of research and industry, highlighting its importance as a fundamental reagent for the creation of novel molecules and materials.

Literature

• Stereocontrolled photodimerization with congested 1,8-bis(4'-anilino)naphthalene templates.

  The Journal of organic chemistry 20101001