6-Chloro-4-methoxynicotinaldehyde is an organic compound characterized by its structural features, which include a chlorinated pyridine ring and an aldehyde functional group. The presence of the chlorine atom at the 6-position and a methoxy group at the 4-position of the nicotinic acid derivative contributes to its unique chemical properties. This compound is typically a pale yellow to light brown solid, exhibiting moderate solubility in organic solvents such as ethanol and dimethyl sulfoxide, while being less soluble in water. It may participate in various chemical reactions, including nucleophilic additions due to the electrophilic nature of the aldehyde group. Additionally, 6-Chloro-4-methoxynicotinaldehyde may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of compounds targeting specific biological pathways. Its synthesis often involves multi-step organic reactions, highlighting its relevance in synthetic organic chemistry. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity and reactivity.

6-Chloro-4-methoxynicotinaldehyde

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CAS 1256823-05-8: 6-Chloro-4-methoxynicotinaldehyde

6-Chloro-4-methoxynicotinaldehyde

Ref: 10-F617167

6-Chloro-4-methoxypyridine-3-carbaldehyde

Ref: 3D-GAC82305

6-Chloro-4-methoxypyridine-3-carbaldehyde

Ref: 54-OR303071

6-Chloro-4-methoxypyridine-3-carbaldehyde

Ref: FT-C15678

6-Chloro-4-methoxypyridine-3-carbaldehyde

Ref: IN-DA00AA9F