CAS 210345-56-5
:Methyl 5-bromo-1H-indole-2-carboxylate
Description:
Methyl 5-bromo-1H-indole-2-carboxylate 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 bromine atom at the 5-position of the indole ring introduces notable reactivity and influences the compound's physical and chemical properties. The carboxylate group, esterified with a methyl group, enhances its solubility in organic solvents and contributes to its potential as a building block in organic synthesis. This compound is often utilized in medicinal chemistry and research due to its biological activity and ability to serve as an intermediate in the synthesis of various pharmaceuticals. Its molecular structure allows for various substitution reactions, making it a versatile compound in synthetic organic chemistry. Additionally, the presence of the bromine atom can facilitate further functionalization, expanding its utility in the development of new chemical entities. Overall, Methyl 5-bromo-1H-indole-2-carboxylate is a significant compound in the field of organic synthesis and medicinal chemistry.
Formula:C10H8BrNO2
InChI:InChI=1/C10H8BrNO2/c1-14-10(13)9-5-6-4-7(11)2-3-8(6)12-9/h2-5,12H,1H3
SMILES:COC(=O)c1cc2cc(ccc2[nH]1)Br
Synonyms:- 1H-Indole-2-carboxylic acid, 5-bromo-, methyl ester
- 5-Bromoindole-2-carboxylic acid methyl ester
- Methyl 5-bromoindole-2-carboxyate
- ZERO/005613
- ZINC00499439
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Found 4 products.
1H-Indole-2-carboxylic acid, 5-bromo-, methyl ester
CAS:Formula:C10H8BrNO2Purity:98%Color and Shape:SolidMolecular weight:254.0800Methyl 5-bromo-1H-indole-2-carboxylate
CAS:Methyl 5-bromo-1H-indole-2-carboxylatePurity:98%Molecular weight:254.08g/molMethyl 5-bromo-1H-indole-2-carboxylate
CAS:Formula:C10H8BrNO2Purity:97%Color and Shape:SolidMolecular weight:254.0835-Bromo-1H-indole-2-carboxylic acid methyl ester
CAS:<p>5-Bromo-1H-indole-2-carboxylic acid methyl ester is a drug that belongs to the class of carboxylates. It has been shown to inhibit the growth of tumor cells in vitro and in vivo. The antitumor activity of this compound may be due to its ability to stabilize planar indole moieties, which are cytotoxic. 5-Bromo-1H-indole-2-carboxylic acid methyl ester interacts with other molecules through intermolecular interactions and can form an indole ring system that has a trifluoromethyl group and a carboxylate group in its structure.</p>Formula:C10H8BrNO2Purity:Min. 95%Molecular weight:254.08 g/mol



