Dichlormid
Appearance
Names | |
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Other names
N,N-diallyl-2,2-dichloroacetamide
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.048.763 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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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).
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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]
It can be synthesized by reacting diallylamine with dichloroacetyl chloride.[3]
References
[edit]- ^ "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.
- ^ Unger, T.A. (1996). Pesticide Synthesis Handbook. William Andrew. p. 17. ISBN 978-0-8155-1853-2. Retrieved 2024-11-22.