5263-87-6
5263-87-6
Chemical Structure
6-Methoxyquinoline
Synonym(s): p-Quinanisole
- CAS No.: 5263-87-6
- Formula:C10H9NO
- Molecular Weight:159.19
IUPAC Name: 6-Methoxyquinoline
InChIKey: HFDLDPJYCIEXJP-UHFFFAOYSA-N
SMILES: COC1=CC2=C(C=C1)N=CC=C2
Biological Activity: 6-Methoxyquinoline consists of a quinoline ring system with a methoxy group attached to the sixth carbon atom. This compound occurs naturally in certain plants, such as tobacco and tea, and has been shown to have biological activities, including antioxidant, anti-inflammatory and antitumor properties. Furthermore, 6-Methoxyquinoline can be used as a building block for the synthesis of other organic compounds, especially those with potential pharmaceutical applications. Due to its ability to bind nucleic acids and proteins, it can also be used as a fluorescent probe in biochemical and biomedical research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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6-Methoxyquinoline | 99.71% | 6-Methoxyquinoline consists of a quinoline ring system with a methoxy group attached to the sixth carbon atom. This compound occurs naturally in certain plants, such as tobacco and tea, and has been shown to have biological activities, including antioxidant, anti-inflammatory and antitumor properties. Furthermore, 6-Methoxyquinoline can be used as a building block for the synthesis of other organic compounds, especially those with potential pharmaceutical applications. Due to its ability to bind nucleic acids and proteins, it can also be used as a fluorescent probe in biochemical and biomedical research. | ||||||||||||||||||||
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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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5-Methoxyquinolin-8-amine | 99.85% | 5-Methoxyquinolin-8-amine is an intermediate. 5-Methoxyquinolin-8-amine can be used to synthesize SND1 inhibitors. 5-Methoxyquinolin-8-amine is applicable to breast cancer-related research. | ||||||||||||||||||||
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5-Methoxyindole | 99.92% | 5-Methoxyindole is an L-tryptophan metabolite with antifungal activity, and also serves as a pharmaceutical intermediate. Metabolites of 5-Methoxyindole exhibit COX-2 inhibitory, anti-inflammatory and anti-tumor activities. 5-Methoxyindole induces morphological distortion of hyphae and conidia, ROS accumulation, apoptosis and cell death in Gaeumannomyces graminis. 5-Methoxyindole can be used in studies related to fungal infections and organic synthesis. | ||||||||||||||||||||
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6-Bromoquinoline | 99.00% | 6-Bromoquinoline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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6-Aminoquinoline | 99.79% | 6-Aminoquinoline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Methoxynaphthalene (Standard) | ≥98% | 2-Methoxynaphthalene (Standard) is the analytical standard of 2-Methoxynaphthalene. This product is intended for research and analytical applications. 2-Methoxynaphthalene can be used to investigate the catalytic benefits of delamination, as well as to study alkali metal-mediated manganization (AMMMn) reactions. | ||||||||||||||||||||
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1-Methoxynaphthalene | 98.59% | 1-Methoxynaphthalene is used as the substrate to investigate the activity of cytochrome c peroxidase (CcP). 1-Methoxynaphthalene also can be used to synthesize prenyl naphthalen-ols. | ||||||||||||||||||||
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6-Methoxynaphthalen-2-ol (Standard) | ≥98% | 6-Methoxynaphthalen-2-ol (Standard) is the analytical standard of 6-Methoxynaphthalen-2-ol. This product is intended for research and analytical applications. | ||||||||||||||||||||
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8-Methoxyquinoline | 8-Methoxyquinoline is a structural analogue of 8-hydroxyquinoline (HY-B1005). 8-Methoxyquinoline does not bind copper. 8-Methoxyquinoline could neither inhibit the chymotrypsin-like activity of the proteasome in breast cancer cell cultures nor induce cancer cell death. 8-Methoxyquinoline can be used in the research of breast cancer. |
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2-Bromo-6-methoxynaphthalene | 99.82% | 2-Bromo-6-methoxynaphthalene is an active intermediate in the production of anti-inflammatory agents like Naproxen and Nabumetone by Heck reaction. 2-Bromo-6-methoxynaphthalene has potential anti-inflammatory properties and Tyrosine-protein inhibitor properties. 2-Bromo-6-methoxynaphthalene can be used for the research of cancer. | ||||||||||||||||||||
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