2-Tert-Butyloxycarbonylamino-6-methylpyridine-3-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in organic synthesis, particularly in Suzuki coupling reactions. The presence of the tert-butoxycarbonyl (Boc) group indicates that this compound can be used as a protecting group for amines, allowing for selective reactions without affecting the amine functionality. The methyl group on the pyridine ring can influence the electronic properties and sterics of the compound, potentially affecting its reactivity and solubility. The pinacol ester moiety is known for its stability and can facilitate the formation of boron-containing compounds. This compound is likely to be a white to off-white solid, soluble in organic solvents, and may exhibit moderate stability under standard laboratory conditions. Its applications may extend to medicinal chemistry and materials science, where boron-containing compounds are of interest for their unique properties. As with all chemical substances, proper handling and safety precautions should be observed due to potential hazards associated with boronic acids and their derivatives.

2-TERT-BUTYLOXYCARBONYLAMINO-6-METHYLPYRIDINE-3-BORONIC ACID PINACOL ESTER

1309982-66-8: 2-Tert-Butyloxycarbonylamino-6-methylpyridine-3-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is significant in organic synthesis, particularly in Suzuki coupling reactions. The presence of the tert-butoxycarbonyl (Boc) group indicates that this compound can be used as a protecting group for amines, allowing for selective reactions without affecting the amine functionality. The methyl group on the pyridine ring can influence the electronic properties and sterics of the compound, potentially affecting its reactivity and solubility. The pinacol ester moiety is known for its stability and can facilitate the formation of boron-containing compounds. This compound is likely to be a white to off-white solid, soluble in organic solvents, and may exhibit moderate stability under standard laboratory conditions. Its applications may extend to medicinal chemistry and materials science, where boron-containing compounds are of interest for their unique properties. As with all chemical substances, proper handling and safety precautions should be observed due to potential hazards associated with boronic acids and their derivatives.

CAS 1309982-66-8

2-TERT-BUTYLOXYCARBONYLAMINO-6-METHYLPYRIDINE-3-BORONIC ACID PINACOL ESTER

tert-Butyl (6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate

Ref: IN-DA009BSU