CAS 324756-80-1
:5-Methoxy-3-formylindole-1-carboxylic acid tert-butyl ester
Description:
5-Methoxy-3-formylindole-1-carboxylic acid tert-butyl 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. This particular compound features a methoxy group (-OCH3) and a formyl group (-CHO) at specific positions on the indole ring, contributing to its reactivity and potential applications in organic synthesis. The tert-butyl ester group provides steric hindrance, which can influence the compound's solubility and reactivity. Typically, compounds like this are of interest in medicinal chemistry and organic synthesis due to their potential biological activity and utility as intermediates in the synthesis of more complex molecules. The presence of functional groups such as the carboxylic acid and the ester can facilitate various chemical reactions, including esterification and hydrolysis. Overall, this compound exemplifies the diverse chemistry associated with indole derivatives, which are known for their wide range of biological activities.
Formula:C15H17NO4
InChI:InChI=1/C15H17NO4/c1-15(2,3)20-14(18)16-8-10(9-17)12-7-11(19-4)5-6-13(12)16/h5-9H,1-4H3
SMILES:CC(C)(C)OC(=O)n1cc(C=O)c2cc(ccc12)OC
Synonyms:- 1H-indole-1-carboxylic acid, 3-formyl-5-methoxy-, 1,1-dimethylethyl ester
- tert-Butyl 3-formyl-5-methoxy-1H-indole-1-carboxylate
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Found 3 products.
5-Methoxy-3-formylindole-1-carboxylic acid tert-butyl ester
CAS:Formula:C15H17NO4Purity:96%Color and Shape:SolidMolecular weight:275.29985-Methoxy-1H-indole-3-carboxaldehyde, N-BOC protected
CAS:<p>5-Methoxy-1H-indole-3-carboxaldehyde, N-BOC protected</p>Purity:98%Molecular weight:275.30g/mol
