3,5-Dichloroaniline
| Names | |
|---|---|
| Other names
1-amino-3,5- dichlorobenzene | |
| Identifiers | |
3D model (JSmol) |
|
| 636492 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.009.954 |
| EC Number |
|
| 363409 | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
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| Properties | |
| C6H5Cl2N | |
| Molar mass | 162.01 g·mol−1 |
| Appearance | colorless solid |
| Density | 1.58 g/cm3 |
| Melting point | 51–53 °C (124–127 °F; 324–326 K) |
| Boiling point | 260 °C (500 °F; 533 K) 741 torr |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H301, H311, H331, H373, H410 | |
| P260, P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P319, P321, P330, P361+P364, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
3,5-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless solid although commercial samples often appear colored. It is produced by hydrogenation of 3,5-dichloronitrobenzene. It is a precursor to the fungicide vinclozolin.