Phthaloyl chloride
From Wikipedia, the free encyclopedia
| Names | |
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| Other names
o-Phthaloyl chloride | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.001.699 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C8H4Cl2O2 | |
| Molar mass | 203.02 g·mol−1 |
| Appearance | colorless oil |
| Melting point | 15.5 °C (59.9 °F; 288.6 K) |
| Boiling point | 135 °C (275 °F; 408 K) 15 torr |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H290, H312, H314, H317, H334, H335 | |
| P233, P234, P260, P264, P264+P265, P271, P272, P280, P284, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P319, P321, P333+P317, P342+P316, P362+P364, P363, P390, P403, 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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Phthaloyl chloride is an organic compound with the formula C6H4(COCl)2. It is one of three isomers, the better known one being terephthaloyl chloride. The third isomer is isophthaloyl chloride. All three compounds are diacid chlorides, and hence they are susceptible to reactions with water (to give back the diacids), alcohols (to give diesters), and amines to give amides or imides.
