CAS 161230-88-2
:1H-Indole-2-carboxylicacid, 3-[(1E)-2-carboxy-2-phenylethenyl]-4,6-dichloro-
Description:
1H-Indole-2-carboxylic acid, 3-[(1E)-2-carboxy-2-phenylethenyl]-4,6-dichloro- is a complex organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This substance features multiple functional groups, including carboxylic acid groups and a dichloro substitution, which can influence its reactivity and solubility. The presence of the phenylethenyl moiety suggests potential for various chemical interactions, making it of interest in medicinal chemistry and organic synthesis. The dichloro substituents may enhance biological activity or alter the compound's electronic properties. Its molecular structure indicates potential applications in pharmaceuticals, particularly in the development of compounds with anti-inflammatory or anticancer properties. Additionally, the compound's solubility and stability can be affected by pH and solvent conditions, which are important considerations for its practical use in research and industry. As with many indole derivatives, it may exhibit interesting biological activities, warranting further investigation.
Formula:C18H11Cl2NO4
Synonyms:- 1H-Indole-2-carboxylicacid, 3-(2-carboxy-2-phenylethenyl)-4,6-dichloro-, (E)-
- 3-((1E)-2-Carboxy-2-phenylethenyl)-4,6-dichloro-1H-indole-2-carboxylic acid
- Mdl 105519
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Found 3 products.
1H-Indole-2-carboxylic acid, 3-[(1E)-2-carboxy-2-phenylethenyl]-4,6-dichloro-
CAS:Formula:C18H11Cl2NO4Purity:99.00%Color and Shape:SolidMolecular weight:376.1902MDL 105519
CAS:MDL 105519 is a selective, non-competitive antagonist of NMDA receptors. It inhibits cyclic GMP accumulation in brain slices, anxiolytic in rat models.Formula:C18H11Cl2NO4Purity:99.67%Color and Shape:SolidMolecular weight:376.19MDL 105519
CAS:<p>Antagonist of NMDA glutamate receptor at glycine binding site</p>Formula:C18H11Cl2NO4Purity:(Hplc-Ms) Min. 98 Area-%Color and Shape:PowderMolecular weight:376.19 g/mol


