1001185-88-1 | 3-Methylsulfonylphenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$20.00	$14.00
250mg	95%	in stock	$25.00	$17.00
1g	95%	in stock	$26.00	$18.00
5g	95%	in stock	$77.00	$54.00
10g	95%	in stock	$153.00	$108.00
25g	95%	in stock	$382.00	$268.00

Description

• Catalog Number: AA01086
• Chemical Name: 3-Methylsulfonylphenylboronic acid pinacol ester
• CAS Number: 1001185-88-1
• Molecular Formula: C13H19BO4S
• Molecular Weight: 282.1636
• MDL Number: MFCD14584690
• SMILES: CC1(C)OB(OC1(C)C)c1cccc(c1)S(=O)(=O)C

Computed Properties

• Complexity: 422
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2

Upstream Synthesis Route

4,4,5,5-Tetramethyl-2-(3-(methylsulfonyl)phenyl)-1,3,2-dioxaborolane is a versatile chemical compound commonly used in chemical synthesis processes. This unique molecule plays a crucial role in modern organic chemistry due to its specific structural properties and reactivity.In chemical synthesis, 4,4,5,5-Tetramethyl-2-(3-(methylsulfonyl)phenyl)-1,3,2-dioxaborolane is frequently employed as a boron-containing building block. Boron-containing compounds are valuable intermediates in organic chemistry as they can participate in various transformations, such as Suzuki-Miyaura cross-coupling reactions. This compound serves as a stable boron source that can be easily incorporated into complex molecular structures, making it a valuable tool for constructing diverse organic molecules.Moreover, the presence of the methylsulfonyl group in the molecule enhances its stability and provides a handle for further derivatization. This feature allows chemists to modify the compound's properties and tailor its reactivity for specific synthetic applications.Overall, the strategic incorporation of 4,4,5,5-Tetramethyl-2-(3-(methylsulfonyl)phenyl)-1,3,2-dioxaborolane in chemical synthesis enables the efficient construction of complex organic molecules with high precision and control. Its versatility and compatibility with various synthetic methodologies make it an indispensable tool for synthetic chemists striving to access novel compounds for academic research or industrial applications.