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Dichlormid

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Dichlormid
Names
Other names N,N-diallyl-2,2-dichloroacetamide
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.048.763 Edit this at Wikidata
EC Number
  • 253-658-8
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H11Cl2NO/c1-3-5-11(6-4-2)8(12)7(9)10/h3-4,7H,1-2,5-6H2Key: YRMLFORXOOIJDR-UHFFFAOYSA-N
SMILES
  • O=C(N(CC=C)CC=C)C(Cl)Cl
Properties
Chemical formula C8H11Cl2NO
Molar mass 208.08 g·mol
Appearance colorless oil
Melting point 5.5 °C (41.9 °F; 278.6 K)
Hazards
GHS labelling:
Pictograms GHS07: Exclamation mark
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 , 100 kPa). Infobox references
Chemical compound

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.

It can be synthesized by reacting diallylamine with dichloroacetyl chloride.

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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