1072945-09-5 | 2-Methylthiophenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$42.00	$30.00
5g	98%	in stock	$98.00	$69.00
10g	98%	in stock	$147.00	$103.00
25g	98%	in stock	$275.00	$193.00
100g	98%	in stock	$760.00	$532.00

Description

• Catalog Number: AE09588
• Chemical Name: 2-Methylthiophenylboronic acid, pinacol ester
• CAS Number: 1072945-09-5
• Molecular Formula: C13H19BO2S
• Molecular Weight: 250.1648
• MDL Number: MFCD05155219
• SMILES: CSc1ccccc1B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 265
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

4,4,5,5-Tetramethyl-2-(2-(methylthio)phenyl)-1,3,2-dioxaborolane, also known by its chemical formula as $name$, is a highly versatile compound widely utilized in chemical synthesis processes. This unique molecule serves as a key building block in organic chemistry, specifically in the field of boron-containing compounds.One of the primary applications of $name$ in chemical synthesis is its role as a boronic acid derivative, making it invaluable in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, is a powerful tool for forming carbon-carbon bonds and is commonly used in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials.Moreover, $name$ is utilized in various other transition metal-catalyzed reactions where the boron moiety plays a crucial role in facilitating selective and efficient bond formations. Its unique structure and reactivity make it a valuable reagent for the construction of diverse molecular architectures with high precision and control.Overall, 4,4,5,5-Tetramethyl-2-(2-(methylthio)phenyl)-1,3,2-dioxaborolane offers chemists a powerful tool for designing and synthesizing intricate organic molecules, thereby enabling advances in drug discovery, materials science, and other chemical disciplines.