CAS 192184-71-7

6-Hydroxy-1H-indole-3-carboxaldehyde

Description:

6-Hydroxy-1H-indole-3-carboxaldehyde, with the CAS number 192184-71-7, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a hydroxyl group (-OH) at the 6-position and an aldehyde group (-CHO) at the 3-position of the indole ring, contributing to its reactivity and potential applications in various chemical reactions. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the presence of the hydroxyl group. The compound is of interest in organic synthesis and medicinal chemistry, as it may serve as a precursor for the synthesis of more complex molecules or as a potential bioactive agent. Its properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. As with many indole derivatives, it may also exhibit interesting biological activities, making it a subject of research in pharmacology and biochemistry.

Formula: C₉H₇NO₂

InChI: InChI=1S/C9H7NO2/c11-5-6-4-10-9-3-7(12)1-2-8(6)9/h1-5,10,12H

InChI key: InChIKey=FAFBOYSDWMRMLQ-UHFFFAOYSA-N

SMILES: C(=O)C=1C=2C(NC1)=CC(O)=CC2

Synonyms:

• 1H-Indole-3-carboxaldehyde, 6-hydroxy-
• 6-Hydroxy-1H-indole-3-carboxaldehyde

1H-Indole-3-carboxaldehyde, 6-hydroxy-

CAS: 192184-71-7

Formula: C₉H₇NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 161.1574

Ref: IN-DA002FP4

6-Hydroxy-1H-indole-3-carbaldehyde

CAS: 192184-71-7

6-Hydroxy-1H-indole-3-carbaldehyde

Purity: 95%

Molecular weight: 161.16g/mol

Ref: 54-OR370135

6-Hydroxy-1H-indole-3-carbaldehyde

CAS: 192184-71-7

Purity: 98%

Molecular weight: 161.1600037

Ref: 10-F788056

6-Hydroxy-1H-indole-3-carbaldehyde

CAS: 192184-71-7

6-Hydroxy-1H-indole-3-carbaldehyde is an anion transporter that has been experimentally shown to inhibit the transport of anions across the plasma membrane. It was found to have significant inhibitory activity against hypouricemia and acetone. The localization of 6-hydroxy-1H-indole-3-carbaldehyde in fungi is unknown, but it has been shown to function as a transporter in macrofungi. 6-Hydroxy-1H-indole-3-carbaldehyde inhibits the uptake of anions by competing with them for the active site on the transporter protein. This mechanism may be due to its ability to bind with cations, which are also transported by these transporters. 6 hydroxy 1H indole 3 carbaldehyde is active against yeast cells and also shows some inhibitory activity against human erythrocytes when high concentrations are used.

Formula: C₉H₇NO₂

Purity: Min. 95%

Molecular weight: 161.16 g/mol

Ref: 3D-SHA18471