4965-36-0
4965-36-0
Chemical Structure
7-Bromoquinoline
- CAS No.: 4965-36-0
- Formula:C9H6BrN
- Molecular Weight:208.06
IUPAC Name: 7-bromoquinoline
InChIKey: XYBSZCUHOLWQQU-UHFFFAOYSA-N
SMILES: BrC1=CC2=C(C=C1)C=CC=N2
Biological Activity: 7-Bromoquinoline is a brominated quinoline derivative. 7-Bromoquinoline can serve as a synthetic intermediate to generate 7-aminoquinoline derivatives. 7-Bromoquinoline can be used to synthesize 7-substituted quinoline derivatives, including quinoline ligands for tau pathology research and neuronal nitric oxide synthase (nNOS) inhibitors[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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7-Bromoquinoline | 99.93% | 7-Bromoquinoline is a brominated quinoline derivative. 7-Bromoquinoline can serve as a synthetic intermediate to generate 7-aminoquinoline derivatives. 7-Bromoquinoline can be used to synthesize 7-substituted quinoline derivatives, including quinoline ligands for tau pathology research and neuronal nitric oxide synthase (nNOS) inhibitors. | ||||||||||||||||||||
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References
- [1]. Broch S, et al. Synthesis and in vitro antiproliferative activities of quinoline derivatives. European journal of medicinal chemistry. 2010 Apr 1;45(4):1657-62.
- [2]. Rombouts FJ, et al. Discovery of N-(Pyridin-4-yl)-1,5-naphthyridin-2-amines as Potential Tau Pathology PET Tracers for Alzheimer's Disease. Journal of medicinal chemistry. 2017 Feb 23;60(4):1272-1291.
- [3]. Cinelli MA, et al. Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors. Journal of medicinal chemistry. 2017 May 11;60(9):3958-3978.
