N-(2-Pyridinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide(CAS: 1383385-64-5)

N-(2-Pyridinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (CAS: 1383385-64-5) is an organic compound with a molecular weight of approximately 412.4 g/mol. It crystallizes in a solid form and is moderately soluble in common organic solvents such as DMF and DMSO. Chemically, it demonstrates reactivity typical of boron-containing compounds, with potential reactivity towards nucleophiles.

N-(2-Pyridinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (CAS: 1383385-64-5) is often synthesized via a Suzuki coupling reaction, where 2-pyridyl boronic acid is coupled with 4-benzoyl-2-pyridineamine in the presence of a palladium catalyst and a base. The synthesis typically yields a high purity product with good selectivity.

N-(2-Pyridinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (CAS: 1383385-64-5) is primarily used in the pharmaceutical industry for its potential medicinal applications. It is also relevant in polymer synthesis and as a reagent in organic chemistry for its boron functionality.

When handling N-(2-Pyridinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (CAS: 1383385-64-5), it is essential to wear appropriate personal protective equipment (PPE) such as gloves and goggles. Handle in a fume hood due to potential inhalation hazards. In case of spill, immediately contain the spill and follow standard safety protocols. Refer to the Safety Data Sheet (SDS) for detailed information and emergency procedures.