CAS 2124-55-2
:indole-4-carboxylic acid
Description:
Indole-4-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring, with a carboxylic acid functional group attached at the fourth position of the indole ring. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the presence of the carboxylic acid group. Indole-4-carboxylic acid is known for its role in various biochemical processes and can serve as a precursor in the synthesis of pharmaceuticals and agrochemicals. It exhibits potential biological activities, including antimicrobial and anti-inflammatory properties, making it of interest in medicinal chemistry. Additionally, its derivatives may be explored for their applications in organic synthesis and material science. As with many indole derivatives, the compound's reactivity can be influenced by the presence of substituents on the indole ring, allowing for diverse chemical transformations.
Formula:C9H6NO2
InChI:InChI=1/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12)/p-1
InChI key:ROGHUJUFCRFUSO-UHFFFAOYSA-N
SMILES:c1cc(c2cc[nH]c2c1)C(=O)[O-]
Synonyms:- 1H-Indole-4-Carboxylic Acid
- 1H-4-Indolecarboxylic Acid
- 4-Indolecarboxylic Acid
- 4-Carboxyindole
- Rarechem Al Be 1201
- Indole-4-Carbocylic Acid
- 4-Indole Carboxylic Acid
- Indole-4-Carboxylicacid
- 1H-Indole-4-Carboxylate
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Indole-4-carboxylic Acid
CAS:Formula:C9H7NO2Purity:>98.0%(GC)(T)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:161.16Indole-4-carboxylic acid
CAS:Indole-4-carboxylic acidFormula:C9H7NO2Purity:98%Molecular weight:161.161H-Indole-4-carboxylic acid
CAS:1H-Indole-4-carboxylic acidFormula:C9H7NO2Purity:98%Color and Shape:Brown SolidMolecular weight:161.15738Indole-4-carboxylic acid
CAS:Indole-4-Carboxylic acid is a molecule that belongs to the group of indole carboxylic acids. It is an organic compound that has a dipole moment and isomers. Indole-4-carboxylic acid can be synthesized by the saponification of indole-7-carboxylic acid, which has two functional groups: a hydroxy group and an amide group. The molecule has a chemical structure with an amide bond between the carboxyl and amino groups at one end, which forms a protonated amide. This protonated amide also has two orientations: trans and cis. The trans orientation is found in human cytochrome P450 and other proteins, while the cis orientation is found in enzymes such as tryptophan synthase, indoleamine 2,3 dioxygenase, or tyrosine hydroxylase.
Formula:C9H7NO2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:161.16 g/mol






