121219-08-7 | 4-Hexyloxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$15.00	$10.00
1g	98%	in stock	$18.00	$12.00
5g	98%	in stock	$40.00	$28.00
10g	98%	in stock	$70.00	$49.00
25g	98%	in stock	$95.00	$66.00
100g	98%	in stock	$283.00	$198.00

Description

• Catalog Number: AD58945
• Chemical Name: 4-Hexyloxyphenylboronic acid
• CAS Number: 121219-08-7
• Molecular Formula: C12H19BO3
• Molecular Weight: 222.0885
• MDL Number: MFCD04039027
• SMILES: CCCCCCOc1ccc(cc1)B(O)O

Computed Properties

• Complexity: 168
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 7

Upstream Synthesis Route

B-[4-(Hexyloxy)phenyl]boronic acid is a versatile compound widely utilized in chemical synthesis due to its unique properties and applications. This particular boronic acid derivative is prized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, a fundamental tool in modern organic synthesis. In this reaction, B-[4-(Hexyloxy)phenyl]boronic acid can be coupled with various aryl halides or pseudohalides under the catalysis of palladium to form biaryl compounds.Furthermore, B-[4-(Hexyloxy)phenyl]boronic acid serves as a crucial building block in the construction of complex organic molecules, offering chemists a powerful tool for the elaboration of molecular structures. Its compatibility with a wide range of functional groups and its stability under various reaction conditions make it an ideal choice for facilitating the synthesis of pharmaceuticals, agrochemicals, materials, and other fine chemicals. With its strategic importance in modern synthetic chemistry, B-[4-(Hexyloxy)phenyl]boronic acid continues to play a key role in advancing the frontiers of chemical research and development.

Literature

• Efficient synthesis and properties of novel near-infrared electrochromic anthraquinone imides.

  Organic letters 20080221