321-38-0
321-38-0
Chemical Structure
1-Fluoronaphthalene
- CAS No.: 321-38-0
- Formula:C10H7F
- Molecular Weight:146.16
IUPAC Name: 1-fluoronaphthalene
InChIKey: CWLKTJOTWITYSI-UHFFFAOYSA-N
SMILES: FC1=C(C=CC=C2)C2=CC=C1
Biological Activity: 1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1-Fluoronaphthalene | 99.56% | 1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake. | ||||||||||||||||||||
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1-Fluoronaphthalene (Standard) | 96.90% | 1-Fluoronaphthalene (Standard) is the analytical standard of 1-Fluoronaphthalene. This product is intended for research and analytical applications. 1-Fluoronaphthalene is an organofluorine compound derived from naphthalene derivatives and fluorinated aromatics. 1-Fluoronaphthalene can be used to synthesize LY248686, a potent inhibitor of serotonin and noradrenaline uptake. | ||||||||||||||||||||
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1-Ethynylnaphthalene | 99.27% | 1-Ethynylnaphthalene is a selective inhibitor of cytochrome P450 1B1. 1-Ethynylnaphthalene is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | ||||||||||||||||||||
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2-Chloronaphthalene | 99.69% | 2-Chloronaphthalene, serving as an intermediate in organic synthesis, is classified as a persistent organic pollutant. 2-Chloronaphthalene can induce apoptosis and autophagy, while inhibiting cell proliferation. 2-Chloronaphthalene leads to cell death through the interplay between autophagy and apoptosis. | ||||||||||||||||||||
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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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1-Naphthalenemethanol (Standard) | 99.99% | 1-Naphthalenemethanol (Standard) is the analytical standard of 1-Naphthalenemethanol (HY-W017241). This product is intended for research and analytical applications. 1-Naphthalenemethanol is a hydroxyl-substituted naphthalene derivative. 1-Naphthalenemethanol can be extracted from the root of Annona senegalensis. 1-Naphthalenemethanol is a photolysis product of 1-napthaleneacetic acid. 1-Naphthalenemethanol, together with PAPS, provides some protection against the irreversible inactivation of AST IV caused by N-OH-2AF. 1-Naphthalenemethanol can be used in antibacterial research. | ||||||||||||||||||||
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Naphthalene-13C10 | Naphthalene-13C10 is 13C labeled Naphthalene-13C10 (HY-W777535). | |||||||||||||||||||||
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2-Naphthol (Standard) | ≥98% | 2-Naphthol (Standard) is the analytical standard of 2-Naphthol. This product is intended for research and analytical applications. 2-Naphthol is a metabolite of naphthalene, catalyzed by cytochrome P450 (CYP) isozymes (CYP 1A1, CYP 1A2, CYP 2A1, CYP 2E1 and CYP 2F2). | ||||||||||||||||||||
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1-Bromonaphthalene | 99.74% | 1-Bromonaphthalene is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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1-Naphthol (Standard) | ≥98% | 1-Naphthol (Standard) is the analytical standard of 1-Naphthol. This product is intended for research and analytical applications. 1-naphthol is an excited state proton transfer (ESPT) fluorescent molecular probe. | ||||||||||||||||||||
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