
Catalog Number	AR00AS2D
Chemical Name	(4-(N,N-Dimethylsulfamoyl)-3,5-dimethylphenyl)boronic acid
CAS Number	1704067-27-5
Molecular Formula	C10H16BNO4S
Molecular Weight	257.11433999999997
MDL Number	MFCD28384285
SMILES	OB(c1cc(C)c(c(c1)C)S(=O)(=O)N(C)C)O

4-(N,N-dimethylsulfamoyl)-3,5-dimethylphenylboronic acid is a versatile reagent widely utilized in chemical synthesis as a key building block in the formation of complex organic molecules. The sulfamoyl group provides a unique functionality that can participate in a variety of reactions to enable the creation of diverse structures.In organic synthesis, this compound serves as a valuable tool for the introduction of the boronic acid moiety, which can undergo various transformations such as Suzuki-Miyaura coupling reactions to form carbon-carbon bonds. Additionally, the sulfamoyl group can act as a directing group in transition metal-catalyzed reactions, allowing for selective functionalization at specific positions within a molecule.Furthermore, the dimethyl substituents on the phenyl ring impart steric effects that influence the reactivity and selectivity of reactions involving this compound. Overall, the strategic incorporation of 4-(N,N-dimethylsulfamoyl)-3,5-dimethylphenylboronic acid in chemical synthesis offers chemists a powerful tool to access an array of structurally complex and biologically relevant compounds.

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Packsize	Purity	Price	Availability	Quantity
250mg	95%	$260.00	Global Stock		Buy Now	Add To Cart
1g	95%	$606.00	Global Stock		Buy Now	Add To Cart

(4-(N,N-Dimethylsulfamoyl)-3,5-dimethylphenyl)boronic acid