CAS 16732-69-7: Ethyl 7-bromo-1H-indole-2-carboxylate
Formula:C11H10BrNO2
InChI:InChI=1/C11H10BrNO2/c1-2-15-11(14)9-6-7-4-3-5-8(12)10(7)13-9/h3-6,13H,2H2,1H3
SMILES:CCOC(=O)c1cc2cccc(c2[nH]1)Br
Synonyms:- 7-Bromoindole-2-Carboxylic Acid Ethyl Ester
- 7-Bromo-1H-Indole-2-Carboxylic Acid Ethyl Ester
- Ethyl 7-Bromoindole-2-Carboxylate
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Found 4 products.
Ethyl 7-bromo-1H-indole-2-carboxylate
CAS:Ethyl 7-bromo-1H-indole-2-carboxylateFormula:C11H10BrNO2Purity:95%Color and Shape: white to light yellow solidMolecular weight:268.11g/molEthyl 7-bromoindole-2-carboxylate
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:268.10998535156251H-Indole-2-carboxylic acid, 7-bromo-, ethyl ester
CAS:Formula:C11H10BrNO2Purity:98%Color and Shape:SolidMolecular weight:268.10667-Bromo-1H-indole-2-carboxylic acid ethyl ester
CAS:7-Bromo-1H-indole-2-carboxylic acid ethyl ester is a tetracyclic compound that is formed by decarboxylation of 7-bromoindole. It has been shown to have constant and unambiguous properties, and crystallizes as a racemic mixture of two enantiomers. It also has the ability to form oxindoles in the presence of tert-butyl alcohol. 7-Bromo-1H-indole-2-carboxylic acid ethyl ester can be synthesized using the following methods: 1) The first step is to react 7-bromoindole with ethyl chloroacetate in an organic solvent such as dichloromethane or chloroform to give 4-(7bromoindol)-5-(ethoxycarbonyl)oxazolidinone. This product can then be reacted with sodiumFormula:C11H10BrNO2Purity:Min. 95%Molecular weight:268.11 g/molRef: 3D-FB56749
Discontinued product
