3-formyl-1H-indole-7-carboxylic acid
$400.00
CAS No.: 317854-65-2
Catalog No.: WLZ1851
Purity: 95%
MF: C10H7NO3
MW: 189.17
Storage: 2-8 degree Celsius
SMILES: C(=O)C1=CNC2=C(C=CC=C12)C(=O)O
Catalog No.: WLZ1851
Purity: 95%
MF: C10H7NO3
MW: 189.17
Storage: 2-8 degree Celsius
SMILES: C(=O)C1=CNC2=C(C=CC=C12)C(=O)O
CAS NO.: 317854-65-2; 3-formyl-1H-indole-7-carboxylic acid. PROPERTIES: This indole derivative features a formyl group and a carboxylic acid group on an indole ring system, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 3-formyl-1H-indole-7-carboxylic acid typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes a conjugated indole system with multiple functional groups that influence the electronic properties of the molecule. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 3-formyl-1H-indole-7-carboxylic acid serves as a valuable intermediate in the synthesis of highly functionalized indole compounds and materials with specific electronic properties. The formyl and carboxylic acid groups provide handles for further functionalization through reactions such as reduction or esterification. In medicinal chemistry, this compound functions as a building block for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The indole framework contributes to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its defined substitution pattern, enabling the development of advanced materials with tailored electronic characteristics.
Reviews
Write Your Own Review