660440-57-3 | 4-(2-Ethoxycarbonylethyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$15.00	$10.00
250mg	97%	in stock	$28.00	$19.00
1g	97%	in stock	$43.00	$31.00
5g	97%	in stock	$203.00	$143.00

Description

• Catalog Number: AH14605
• Chemical Name: 4-(2-Ethoxycarbonylethyl)phenylboronic acid
• CAS Number: 660440-57-3
• Molecular Formula: C11H15BO4
• Molecular Weight: 222.0454
• MDL Number: MFCD04115652
• SMILES: CCOC(=O)CCc1ccc(cc1)B(O)O

Computed Properties

• Complexity: 212
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6

Upstream Synthesis Route

(4-(3-Ethoxy-3-oxopropyl)phenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in the formation of complex organic molecules. This compound serves as an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, (4-(3-Ethoxy-3-oxopropyl)phenyl)boronic acid can participate in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. This reaction is essential in the construction of carbon-carbon bonds, allowing for the synthesis of various functionalized aromatic compounds with high efficiency and selectivity.Furthermore, this boronic acid derivative can be utilized in the formation of heterocyclic compounds through palladium-catalyzed coupling reactions. By incorporating this compound into the organic synthesis process, chemists can access a wide range of structurally diverse molecules that are essential in drug discovery and material science.Overall, the application of (4-(3-Ethoxy-3-oxopropyl)phenyl)boronic acid in chemical synthesis enables the efficient construction of complex organic molecules with diverse functionalities, making it an indispensable tool for synthetic chemists in the development of novel compounds for various applications.