
Catalog Number	AR00SP0E
Chemical Name	N-[2-chloro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide
CAS Number	2246836-43-9
Molecular Formula	C13H19BClNO4S
Molecular Weight	331.6233
MDL Number	MFCD32206453
SMILES	Clc1ccc(cc1NS(=O)(=O)C)B1OC(C(O1)(C)C)(C)C

1. N-(2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide is a versatile reagent widely used in chemical synthesis for reactions that involve the selective functionalization of aromatic compounds.2. It serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to introduce specific functional groups with high regioselectivity and efficiency.3. The presence of the boron moiety in this compound enables it to participate in Suzuki-Miyaura cross-coupling reactions, a powerful tool in organic synthesis for forming carbon-carbon bonds. This reaction has broad applicability in the construction of complex molecules.4. Additionally, the sulfonamide group in this compound can serve as a directing group in transition metal-catalyzed C-H functionalization reactions, allowing for the selective modification of specific carbon-hydrogen bonds in the presence of others.5. Overall, N-(2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamide plays a crucial role in modern organic synthesis by enabling the efficient and controlled functionalization of aromatic compounds for the creation of diverse and valuable chemical products.