CAS 325800-39-3
:tert-butyl 5-bromo-3-formyl-1H-indole-1-carboxylate
Description:
Tert-butyl 5-bromo-3-formyl-1H-indole-1-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. This compound features a tert-butyl ester group, which enhances its lipophilicity and stability. The presence of a bromine atom at the 5-position of the indole ring introduces a halogen substituent that can influence the compound's reactivity and biological activity. Additionally, the formyl group at the 3-position serves as a reactive aldehyde functional group, making it a potential candidate for further chemical transformations. The carboxylate moiety contributes to the compound's acidity and can participate in various chemical reactions, such as esterification or amidation. Overall, this compound's unique structural features make it of interest in synthetic organic chemistry and potentially in medicinal chemistry for the development of new pharmaceuticals. Its CAS number, 325800-39-3, allows for easy identification and reference in chemical databases.
Formula:C14H14BrNO3
InChI:InChI=1/C14H14BrNO3/c1-14(2,3)19-13(18)16-7-9(8-17)11-6-10(15)4-5-12(11)16/h4-8H,1-3H3
SMILES:CC(C)(C)OC(=O)n1cc(C=O)c2cc(ccc12)Br
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Found 3 products.
5-BROMO-3-FORMYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS:Formula:C14H14BrNO3Purity:95%Color and Shape:SolidMolecular weight:324.16995-Bromo-1H-indole-3-carboxaldehyde, N-BOC protected
CAS:5-Bromo-1H-indole-3-carboxaldehyde, N-BOC protectedPurity:97%Color and Shape:PowderMolecular weight:324.17g/mol1-Boc-5-Bromo-3-formylindole
CAS:Formula:C14H14BrNO3Purity:95%Color and Shape:No data available.Molecular weight:324.174


