CAS 868656-97-7
:1H-Indole-3-carboxylic acid, 6-bromo-, methyl ester
Description:
1H-Indole-3-carboxylic acid, 6-bromo-, methyl ester is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a carboxylic acid group at the 3-position and a bromine atom at the 6-position, along with a methyl ester functional group, contributes to its unique reactivity and properties. This compound is typically used in organic synthesis and medicinal chemistry due to its potential biological activity, particularly in the development of pharmaceuticals. Its molecular structure allows for various interactions, making it a candidate for studies related to enzyme inhibition or receptor binding. The methyl ester form enhances its solubility and stability, which can be advantageous in biological assays. As with many brominated compounds, it may exhibit specific reactivity patterns, including electrophilic substitution reactions. Overall, 1H-Indole-3-carboxylic acid, 6-bromo-, methyl ester is a versatile compound with applications in research and development within the field of chemistry.
Formula:C10H8BrNO2
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Found 5 products.
Methyl 6-bromo-1H-indole-3-carboxylate
CAS:Formula:C10H8BrNO2Purity:96%Color and Shape:SolidMolecular weight:254.0800Methyl 6-bromo-1H-indole-3-carboxylate
CAS:Methyl 6-bromo-1H-indole-3-carboxylatePurity:≥95%Molecular weight:254.08g/molMethyl 6-bromoindole-3-carboxylate
CAS:<p>Methyl 6-bromoindole-3-carboxylate</p>Purity:98%Molecular weight:254.08g/molMethyl 6-bromo-1H-indole-3-carboxylate
CAS:<p>1H-Indole-3-Carboxylic Acid,6-Bromo-,Methyl Ester (Methyl 6-bromo-1H-indole-3-carboxylate) is a marine derived natural products found in Smenospongia sp.</p>Formula:C10H8BrNO2Purity:97.18% - 98.74%Color and Shape:SolidMolecular weight:254.08Methyl 6-bromo-1H-indole-3-carboxylate
CAS:Formula:C10H8BrNO2Purity:95%Color and Shape:SolidMolecular weight:254.083



