348640-06-2
Chemical Structure
4-Bromo-7-azaindole
- CAS No.: 348640-06-2
- Formula:C7H5BrN2
- Molecular Weight:197.03
IUPAC Name: 4-bromo-1H-pyrrolo[2,3-b]pyridine
InChIKey: LEZHTYOQWQEBLH-UHFFFAOYSA-N
SMILES: BrC1=CC=NC2=C1C=CN2
Biological Activity: 4-Bromo-7-azaindole is a brominated derivative of 7-azaindole. 4-Bromo-7-azaindole serves as a substrate for palladium-catalyzed C-N and C-O cross-coupling reactions, reacting with amides, amines, amino acid esters and phenols[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
4-Bromo-7-azaindole | 99.55% | 4-Bromo-7-azaindole is a brominated derivative of 7-azaindole. 4-Bromo-7-azaindole serves as a substrate for palladium-catalyzed C-N and C-O cross-coupling reactions, reacting with amides, amines, amino acid esters and phenols. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Morzyk-Ociepa B, et al. Crystal structures, vibrational spectra and DFT calculations of five halogeno-derivatives of 7-azaindole (3Br7AI, 4Br7AI, 4Cl7AI, 3Br4Cl7AI and 5Br3Cl7AI): A comparative study. Journal of Molecular Structure. 2018;Jan15;1152:386-98.
- [2]. Surasani R, et al. Palladium-catalyzed C-N and C-O bond formation of N-substituted 4-bromo-7-azaindoles with amides, amines, amino acid esters and phenols. Beilstein J Org Chem. 2012;8:2004-2018. [Content Brief]
Keywords