2-Chloro-4-methylpyridine-5-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound features a chlorine atom and a methyl group at specific positions on the pyridine ring, which influences its reactivity and solubility. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chlorine atom can enhance the electrophilicity of the pyridine ring, facilitating nucleophilic substitution reactions. Additionally, the methyl group can affect the steric and electronic properties of the molecule, potentially influencing its interactions with biological targets. This compound is typically used in the synthesis of complex organic molecules and may serve as a building block in the development of pharmaceuticals or agrochemicals. As with many boronic acids, it is important to handle this substance with care, as it may exhibit specific reactivity under certain conditions.

2-Chloro-4-methylpyridine-5-boronic acid

913836-08-5: (2-Chloro-4-methyl-pyridin-5-yl)boronic acid, (6-Chloro-4-Methyl-3-Pyridyl)Boronic Acid, (6-Chloro-4-methylpyridin-3-yl)boronic acid, 2-Chloro-4-picoline-5-boronic acid, 6-Chloro-4-methylpyridine-3-boronic acid, B-(6-Chloro-4-methyl-3-pyridinyl)boronic acid, Boronic acid, (6-chloro-4-methyl-3-pyridinyl)-, Boronic acid, B-(6-chloro-4-methyl-3-pyridinyl)-

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CAS 913836-08-5: 2-Chloro-4-methylpyridine-5-boronic acid

(6-Chloro-4-methylpyridin-3-yl)boronic acid

Ref: 3D-FC139815

2-Chloro-4-methylpyridine-5-boronic acid

Ref: IN-DA00GSKG

2-Chloro-4-methyl-5-pyridineboronic acid

Ref: 10-F076875

6-Chloro-4-methylpyridine-3-boronic acid

Ref: 54-OR3766

2-Chloro-4-methylpyridine-5-boronic acid

Ref: FT-C10086