Dichlormid

Last updated
Dichlormid
Dichloramid.svg
Names
Other names
N,N-diallyl-2,2-dichloroacetamide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.048.763 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 253-658-8
KEGG
PubChem CID
UNII
  • 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
  • O=C(N(CC=C)CC=C)C(Cl)Cl
Properties
C8H11Cl2NO
Molar mass 208.08 g·mol−1
Appearancecolorless oil
Melting point 5.5 °C (41.9 °F; 278.6 K)
Hazards
GHS labelling: [1]
GHS-pictogram-exclam.svg
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).

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

  1. ↑ "Dichlormid". pubchem.ncbi.nlm.nih.gov.
  2. ↑ 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.
  3. ↑ Unger, T.A. (1996). Pesticide Synthesis Handbook. William Andrew. p. 17. ISBN   978-0-8155-1853-2 . Retrieved 2024-11-22.
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