Dichlormid

Dichlormid
Names
	Other names N,N-diallyl-2,2-dichloroacetamide
Identifiers
CAS Number	37764-25-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:81956;
ChEMBL	ChEMBL2251310;
ChemSpider	34686;
ECHA InfoCard	100.048.763
EC Number	253-658-8;
KEGG	C18782;
PubChem CID	37829;
UNII	E901J4382O;
CompTox Dashboard (EPA)	DTXSID4027997 ;
	InChI InChI=1S/C8H11Cl2NO/c1-3-5-11(6-4-2)8(12)7(9)10/h3-4,7H,1-2,5-6H2 Key: YRMLFORXOOIJDR-UHFFFAOYSA-N;
	SMILES O=C(N(CC=C)CC=C)C(Cl)Cl;
Properties
Chemical formula	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:
Pictograms
Signal word	Warning
Hazard statements	H302, H315, H332
Precautionary statements	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]

It can be synthesized by reacting diallylamine with dichloroacetyl chloride.^[3]

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.
^ Unger, T.A. (1996). Pesticide Synthesis Handbook. William Andrew. p. 17. ISBN 978-0-8155-1853-2. Retrieved 2024-11-22.