
Catalog Number	AR01DUFI
Chemical Name	N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide
CAS Number	874290-96-7
Molecular Formula	C18H27BN2O3
Molecular Weight	330.2296
MDL Number	MFCD31716300
SMILES	O=C(N1CCCCC1)Nc1ccc(cc1)B1OC(C(O1)(C)C)(C)C

N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide is a valuable compound widely utilized in chemical synthesis. This compound serves as a versatile building block in the creation of complex organic molecules due to its ability to undergo various chemical transformations. Its unique structure containing a boronate ester and a piperidine moiety enables it to participate in key reactions such as cross-coupling reactions, Suzuki-Miyaura coupling, and C-H activation.In organic synthesis, N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide plays a crucial role as a key intermediate for the introduction of functional groups, facilitating the construction of diverse molecular scaffolds. Its compatibility with a wide range of reaction conditions and its stability make it a preferred choice for chemists seeking to streamline their synthetic pathways and access complex target molecules efficiently.By incorporating N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide into their synthetic strategies, researchers and industrial chemists can enhance the efficiency and versatility of their chemical transformations, enabling the synthesis of novel compounds with potential applications in pharmaceuticals, agrochemicals, materials science, and other fields of chemical research.