1,8-Naphthalic anhydride
Chemical compound
From Wikipedia, the free encyclopedia
1,8-Naphthalic anhydride is an organic compound with the formula C10H6(C2O3). It is one of three isomers of naphthalic anhydride, the other two being the 1,2- and the 2,3-derivatives. The 1,8-isomer is prepared by aerobic oxidation of acenaphthene.[1] 2,6-naphthalenedicarboxylic acid can be prepared from this anhydride.[2] 1,8-Naphthalic anhydride is a precursor to the 4-chloro and 4,5-dichloro derivatives. These chloride groups are susceptible to displacement by amines and alkoxides,[3] giving rise, ultimately, to a large family of naphthalimides, which are used as optical brighteners.[4]
| Names | |
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| Preferred IUPAC name
1H,3H-Naphtho[1,8-cd]pyran-1,3-dione | |
| Other names
1,8-Naphthalenedicarboxylic acid anhydride | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.256 |
| EC Number |
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| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C12H6O3 | |
| Molar mass | 198.177 g·molâ1 |
| Appearance | white solid |
| Melting point | 269â276 °C (516â529 °F; 542â549 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H317, H319, H335 | |
| P261, P264, P271, P272, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Derivatives include: Alrestatin,...
