1146169-44-9 | 4-[(2-methoxyethoxy)methyl]phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$106.00	$75.00
1g	98%	in stock	$251.00	$176.00
5g	98%	in stock	$760.00	$532.00
10g	98%	in stock	$1,319.00	$923.00
25g	98%	in stock	$2,625.00	$1,837.00

Description

• Catalog Number: AA19039
• Chemical Name: 4-[(2-methoxyethoxy)methyl]phenylboronic acid
• CAS Number: 1146169-44-9
• Molecular Formula: C10H15BO4
• Molecular Weight: 210.0347
• MDL Number: MFCD14687278
• SMILES: COCCOCc1ccc(cc1)B(O)O

Computed Properties

• Complexity: 158
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6

Upstream Synthesis Route

The product $name$ is a versatile chemical compound used in various chemical synthesis reactions, particularly in the field of organic chemistry. With its unique structure of (4-((2-Methoxyethoxy)methyl)phenyl)boronic acid, it serves as a valuable building block for the construction of more complex molecules.In chemical synthesis, (4-((2-Methoxyethoxy)methyl)phenyl)boronic acid acts as a boronic acid derivative, which is known for its ability to participate in Suzuki-Miyaura cross-coupling reactions. This reaction is a highly efficient and widely used method for forming carbon-carbon bonds in the presence of palladium catalysts. By incorporating (4-((2-Methoxyethoxy)methyl)phenyl)boronic acid into the reaction system, chemists can facilitate the coupling of this boronic acid with other organic compounds to create new substances with tailored properties.Furthermore, (4-((2-Methoxyethoxy)methyl)phenyl)boronic acid can also be utilized in other types of transformations, such as metal-catalyzed C-H activation reactions and Buchwald-Hartwig amination reactions. These diverse applications highlight the importance of (4-((2-Methoxyethoxy)methyl)phenyl)boronic acid as a valuable reagent in synthetic chemistry, enabling the efficient and precise construction of complex molecules with specific functionalities.