4433-63-0 | Ethylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$16.00	$11.00
5g	95%	in stock	$18.00	$12.00
10g	95%	in stock	$21.00	$15.00
25g	95%	in stock	$49.00	$34.00
100g	95%	in stock	$146.00	$102.00

Description

• Catalog Number: AB74112
• Chemical Name: Ethylboronic acid
• CAS Number: 4433-63-0
• Molecular Formula: C2H7BO2
• Molecular Weight: 73.8868
• MDL Number: MFCD01074536
• SMILES: CCB(O)O

Computed Properties

• Complexity: 21.6
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

Ethylboronic acid is a versatile compound that finds widespread application in chemical synthesis. One of its key uses is in the formation of carbon-carbon bonds through various coupling reactions. This compound serves as a valuable building block in the construction of complex organic molecules, especially in the field of pharmaceuticals and agrochemicals. Additionally, Ethylboronic acid is utilized in Suzuki-Miyaura cross-coupling reactions, where it reacts with organic halides or pseudo-halides in the presence of a palladium catalyst to form biaryl compounds. Its compatibility with a variety of functional groups makes it a valuable tool for synthetic chemists seeking efficient and selective bond-forming reactions. Furthermore, Ethylboronic acid has been employed in the synthesis of materials for use in electronics, such as organic light-emitting diodes (OLEDs) and organic semiconductors. Its ability to participate in diverse chemical transformations and its importance in the construction of complex molecules highlight the significance of Ethylboronic acid in modern organic synthesis.

Literature

• Upregulation of arginase-II contributes to decreased age-related myocardial contractile reserve.

  European journal of applied physiology 20120801