Dillapiole

Dillapiole
Names
	IUPAC names 1-Allyl-2,3-dimethoxy-4,5-; (methylenedioxy)benzene
Identifiers
CAS Number	484-31-1 [citation needed] ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL470874 ;
ChemSpider	9814 ;
ECHA InfoCard	100.149.911
KEGG	C10449 ;
PubChem CID	10231;
CompTox Dashboard (EPA)	DTXSID80862007 ;
	InChI 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 Key: LIKYNOPXHGPMIH-UHFFFAOYSA-N ; 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;
	SMILES O1c2cc(c(OC)c(OC)c2OC1)CC=C;
Properties
Chemical formula	C12H14O4
Molar mass	222.24 g/mol
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). verify (what is ?) Infobox references

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]

No carcinogenicity was detected with parsley apiol or dill apiol in mice.^[4]

References

^ Azeez, Shamina (2008). Chemistry of Spices. Calicut, Kerala, India: Biddles Ltd. pp. 227–241 [230]. ISBN 9781845934057.
^ Santos, P. A. G.; Figueiredo, A. C.; Lourenço, P. M. L.; Barroso, J. G.; Pedro, L. G.; Oliveira, M. M.; Schripsema, J.; Deans, S. G.; Scheffer, J. J. C. (2002). "Hairy root cultures of Anethum graveolens (Dill): Establishment, growth, time-course study of their essential oil and its comparison with parent plant oils" (pdf). Biotechnology Letters. 24 (12): 1031–1036. doi:10.1023/A:1015653701265.
^ Shulgin, A. T.; Sargent, T. (1967). "Psychotrophic phenylisopropylamines derived from apiole and dillapiole". Nature. 215 (5109): 1494–1495. doi:10.1038/2151494b0. PMID 4861200.
^ Phillips DH; Reddy MV; Randerath K (1984). "32P-post-labelling analysis of DNA adducts formed in the livers of animals treated with safrole, estragole and other naturally-occurring alkenylbenzenes. II. Newborn male B6C3F1 mice". Carcinogenesis. Vol. 5, no. 12. pp. 1623–8.