
Catalog Number	AR01DUFO
Chemical Name	(3-((4-Methoxyphenyl)carbamoyl)phenyl)boronic acid
CAS Number	874459-99-1
Molecular Formula	C14H14BNO4
Molecular Weight	271.0763
MDL Number	MFCD28167459
SMILES	COc1ccc(cc1)NC(=O)c1cccc(c1)B(O)O

The (3-((4-Methoxyphenyl)carbaMoyl)phenyl)boronic acid is a crucial compound in chemical synthesis, specifically in the field of organic chemistry. It serves as a versatile building block for the construction of various functional molecules due to its unique structural properties.One of the primary applications of this compound is in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative that can undergo a palladium-catalyzed coupling reaction with organic halides or pseudohalides. This process enables the formation of biaryl compounds, which are essential structural motifs found in numerous natural products, pharmaceuticals, and materials.Furthermore, (3-((4-Methoxyphenyl)carbaMoyl)phenyl)boronic acid also finds utility in the preparation of advanced materials, such as polymers, liquid crystals, and semiconductors, through various synthetic methodologies. Its ability to functionalize aromatic systems with boronic acid functionality opens up a wide range of possibilities for molecular design and structure-property relationships.In summary, the (3-((4-Methoxyphenyl)carbaMoyl)phenyl)boronic acid plays a pivotal role in modern chemical synthesis by facilitating the creation of complex organic molecules with tailored properties and functionalities. Its versatility and reactivity make it an indispensable tool for researchers and chemists working in the development of novel compounds and materials.