CAS 1196152-22-3

6-Chloro-4-hydroxy-3-pyridinecarboxaldehyde

Description:

6-Chloro-4-hydroxy-3-pyridinecarboxaldehyde is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. This compound features a chloro substituent at the 6-position and a hydroxy group at the 4-position, along with an aldehyde functional group at the 3-position of the pyridine ring. The presence of these functional groups contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The chloro group can participate in nucleophilic substitution reactions, while the aldehyde can undergo condensation reactions and serve as a precursor for various derivatives. The hydroxy group may also influence the compound's solubility and hydrogen bonding capabilities. Overall, 6-Chloro-4-hydroxy-3-pyridinecarboxaldehyde is of interest in research for its potential biological activities and as a building block in the synthesis of more complex molecules. Its specific properties, such as melting point, boiling point, and solubility, would need to be referenced from experimental data or literature for precise applications.

Formula: C₆H₄ClNO₂

InChI: InChI=1S/C6H4ClNO2/c7-6-1-5(10)4(3-9)2-8-6/h1-3H,(H,8,10)

InChI key: InChIKey=QUTHIVPADSLFBK-UHFFFAOYSA-N

SMILES: C(=O)C=1C(O)=CC(Cl)=NC1

Synonyms:

• 3-Pyridinecarboxaldehyde, 6-chloro-4-hydroxy-
• 6-Chloro-4-hydroxy-3-pyridinecarboxaldehyde

6-Chloro-4-hydroxynicotinaldehyde

CAS: 1196152-22-3

6-Chloro-4-hydroxynicotinaldehyde

Purity: 95%

Molecular weight: 157.56g/mol

Ref: 54-OR1064808