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1 References  














Dichlormid






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From Wikipedia, the free encyclopedia
 


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=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

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:[1]

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 [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[edit]

  1. ^ "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.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Dichlormid&oldid=1192535660"

    Categories: 
    Herbicides
    Allylamines
    Acetamides
    Organochlorides
    Hidden categories: 
    Articles without InChI source
    ECHA InfoCard ID from Wikidata
    Chembox having GHS data
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 29 December 2023, at 22:33 (UTC).

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