Dillapiole

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Dillapiole
Skeletal formula
Ball-and-stick model
Names
Preferred IUPAC name
4,5-Dimethoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole
Other names
6-Allyl-4,5-dimethoxybenzo[d][1,3]dioxole
1-Allyl-2,3-dimethoxy-4,5-(methylenedioxy)benzene
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
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EC Number
  • 621-020-1
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KEGG
UNII
  • {{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
  • InChI=1S/C12H14O4/c1-4-5-8-6-9-11(16-7-15-9)12(14-3)10(8)13-2/h4,6H,1,5,7H2,2-3H3 checkY
    Key: LIKYNOPXHGPMIH-UHFFFAOYSA-N checkY
  • InChI=1/C12H14O4/c1-4-5-8-6-9-11(16-7-15-9)12(14-3)10(8)13-2/h4,6H,1,5,7H2,2-3H3
    Key: LIKYNOPXHGPMIH-UHFFFAOYAI
  • O1c2cc(c(OC)c(OC)c2OC1)CC=C
Properties
C12H14O4
Molar mass 222.240 g·mol−1
Density 1.163 g/cm3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Dillapiole is an organic chemical compound and essential oil commonly extracted from dill weed, though it can be found in a variety of other plants such as fennel root.[1] This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring.[2][3] Dillapiole works synergically with certain insecticides like pyrethrins similarly to piperonyl butoxide, which likely results from inhibition of the MFO enzyme of insects.[4]

No carcinogenicity was detected with parsley apiol or dill apiol in mice.[5]

See also

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References

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  4. ^ IN patent 128,129, Mankombu Sambasivan Swaminathan, "Improvements in or relating to methylenedioxyphenyl derivatives", published Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)., issued Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value). 
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See also

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