|  | |
| Names | |
|---|---|
| Other names N,N-diallyl-2,2-dichloroacetamide | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.048.763 | 
| EC Number | 
 | 
| KEGG | |
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C8H11Cl2NO | |
| Molar mass | 208.08 g·mol−1 | 
| Appearance | colorless oil | 
| Melting point | 5.5 °C (41.9 °F; 278.6 K) | 
| Hazards | |
| GHS labelling:[1] | |
|  | |
| Warning | |
| H302, H315, H332 | |
| P261, P264, P270, P271, P280, P301+P317, P302+P352, P304+P340, P317, P321, P330, P332+P317, P362+P364, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Dichlormid is an organic compound with the formula Cl2CHCON(CH2C=CH2)2. The compound can be classified as the amide of diallylamine and dichloroacetic acid. It is an herbicide safener for use with maize.[2]
References
- ↑ "Dichlormid". pubchem.ncbi.nlm.nih.gov.
- ↑ Riechers, Dean E.; Kreuz, Klaus; Zhang, Qin (2010). "Detoxification without Intoxication: Herbicide Safeners Activate Plant Defense Gene Expression". Plant Physiology. 153 (1): 3–13. doi:10.1104/pp.110.153601. PMC 2862420. PMID 20237021.
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