Phenylnaphthalenes
Phenylnaphthalenes are a class of organic compounds that belong to the family of polycyclic aromatic hydrocarbons (PAHs). These compounds contain one or more phenyl rings attached to a naphthalene core, resulting in unique structural and chemical properties. Phenylnaphthalenes exhibit diverse applications due to their physicochemical characteristics, including use as intermediates in the synthesis of dyes, pharmaceuticals, and plastics. Additionally, they are known for their thermal stability and potential as flame-retardant additives. The presence of phenyl groups introduces reactive sites that can facilitate various chemical reactions, making phenylnaphthalenes valuable in industrial processes. However, due to their structural complexity and aromatic nature, these compounds must be handled with caution in environments where safety and environmental impact are critical concerns.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Trigoxyphin X | 1967777-58-7 | C24H18O4 |
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2,4,6-Trihydroxy-9-phenyl-1H-phenalen-1-one; 4,6-Di-Me ether | 1799702-68-3 | C21H16O4 |
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2,5,6-Trihydroxy-7(9)-phenyl-1H-phenalen-1-one; 3-Chloro, 6-Me ether | 1801340-30-6 | C20H13ClO4 |
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2,5,6-Trihydroxy-7(9)-phenyl-1H-phenalen-1-one; 1-O-(6-O-Malonyl-β-D-glucopyranoside) | 1393689-35-4 | C28H24O12 |
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2,5,6-Trihydroxy-7(9)-phenyl-1H-phenalen-1-one; 2-Me ether, 1-O-(6-O-malonyl-β-D-glucopyranoside) | 1393689-37-6 | C29H26O12 |
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Wailupemycin G; 3'-Me ether | 2154433-65-3 | C22H16O5 |
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Wailupemycin H | 2242962-75-8 | C43H30O11 |
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Wailupemycin H; 6-Epimer | 2242962-76-9 | C43H30O11 |
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Ningalin C; 3',3'',3''',5-Tetradeoxy | 1593822-12-8 | C32H23NO6 |
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Ningalin G | 1382192-96-2 | C40H27NO12 |
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