1-Nitronaphthalene
Chemical compound
From Wikipedia, the free encyclopedia
1-Nitronaphthalene is an organic compound with the formula C10H7NO2. It is one of two isomers of nitronaphthalene. A pale yellow, sublimable solid, 1-nitronaphthalene is the main product of the direct nitration of naphthalene. It is an intermediate in the production of naphthylamine, a precursor to dyes.[3] The conversion to the amine is effected by hydrogenation.[4]
| Names | |
|---|---|
| Preferred IUPAC name
1-Nitronaphthalene | |
| Other names
α-Nitronaphthalene | |
| Identifiers | |
3D model (JSmol) |
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| 1867714 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.531 |
| EC Number |
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| KEGG | |
PubChem CID |
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| UNII | |
| UN number | 2538 |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H7NO2 | |
| Molar mass | 173.171 g·molâ1 |
| Appearance | pale yellow solid |
| Density | 1.223 g/cm3[1] |
| Melting point | 53â57 °C (127â135 °F; 326â330 K)[1] |
| Boiling point | 304 °C (579 °F; 577 K)[1] |
| releases toxic and flammable gas[2] | |
| Vapor pressure | 0.00064 hPa[1] |
| Hazards[1] | |
| GHS labelling: | |
| Warning | |
| H228, H302, H411 | |
| P210, P240, P241, P264, P270, P273, P280, P301+P312+P330, P370+P378, P391, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 164 °C (327 °F; 437 K) (closed cup) |
| 450 °C (842 °F; 723 K)[2] | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
350 mg/kg (oral, rat) |
LC50 (median concentration) |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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