1217501-53-5 | 2-Methyl-4-(morpholinosulfonyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$30.00	$21.00
250mg	96%	in stock	$36.00	$25.00
1g	96%	in stock	$120.00	$84.00
5g	96%	in stock	$573.00	$402.00
10g	96%	in stock	$946.00	$662.00

Description

• Catalog Number: AA53978
• Chemical Name: 2-Methyl-4-(morpholinosulfonyl)phenylboronic acid
• CAS Number: 1217501-53-5
• Molecular Formula: C11H16BNO5S
• Molecular Weight: 285.12444
• MDL Number: MFCD13195673
• SMILES: OB(c1ccc(cc1C)S(=O)(=O)N1CCOCC1)O

Computed Properties

• Complexity: 390
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

The (2-Methyl-4-(morpholinosulfonyl)phenyl)boronic acid, commonly referred to as $name$, is a versatile chemical compound with a wide range of applications in chemical synthesis. This boronic acid derivative plays a crucial role as a valuable building block in the field of organic chemistry.One of the key applications of $name$ in chemical synthesis is its utility as a cross-coupling reagent in the formation of carbon-carbon and carbon-heteroatom bonds. Its boronic acid functionality allows for the selective activation of the phenyl ring, leading to controlled reactions with various electrophiles. This property makes it an essential component in Suzuki-Miyaura cross-coupling reactions, enabling the creation of complex molecular structures.Moreover, the presence of the morpholinosulfonyl group in the structure of $name$ provides enhanced stability and selectivity during reactions, making it a valuable tool for the synthesis of pharmaceutical intermediates and agrochemicals. The unique combination of boronic acid and morpholinosulfonyl functionalities in $name$ offers chemists a powerful platform for the construction of diverse organic molecules with high efficiency and precision.