Naphthalenes
Naphthalenes are a class of polycyclic aromatic hydrocarbons (PAHs) derived from benzene rings fused together to form a bicyclic structure. They exist in two isomeric forms: alpha-naphthalene and beta-naphthalene, which differ in the positioning of their substituents relative to the point of fusion between the two benzene rings. These compounds are found naturally but can also be produced synthetically for various applications.
Naphthalenes exhibit unique physical properties due to their crystalline structure, including high melting points and low solubility in water. They are widely used as raw materials in the production of dyes, insecticides, and synthetic rubber. Additionally, naphthalene derivatives find application in pharmaceuticals, fragrances, and as intermediates in organic synthesis.
Safety considerations must be observed when handling naphthalenes due to their potential toxic effects on human health. They are classified as irritants and may cause skin irritation or respiratory issues if not properly handled. Proper protective equipment, such as gloves and respirators, should be used during manipulation and storage of these compounds.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Cyclobuta[b]naphthalen-1(2H)-one | 89185-31-9 | C12H8O |
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Naphthalene, didecyl- | 90454-22-1 | C30H48 |
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Naphthalene, 1,2,6,7-tetramethyl- | 99486-63-2 | C14H16 |
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2-Naphthalenecarboxaldehyde,1-chloro-3,4-dihydro-6,7-dimethoxy- | 885279-10-7 | C13H13ClO3 |
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2-Naphthalenesulfinicacid, 6-methyl- | 801141-06-0 | C11H10O2S |
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2-Naphthaleneaceticacid, 1-amino- | 858438-26-3 | C12H11NO2 |
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1-Fluoro-6-methoxy-naphthalene | 853192-64-0 | C11H9FO |
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(2-methoxynaphthalen-1-yl)methylhydrazine | 887592-83-8 | C12H14N2O |
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Naphthalene, 7-bromo-1-(bromomethyl)- | 81830-68-4 | C11H8Br2 |
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2-Butenal, 3-(2-naphthalenyl)-, (E)- | 81826-92-8 | C14H12O |
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