|Preferred IUPAC name
1-Allyl-2,3-dimethoxy-4,5-(methylenedioxy)benzene (no longer recommended)
3D model (Jmol)
|Molar mass||222.24 g/mol|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
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. This compound is closely related to apiole, having a methoxy group positioned differently on the benzene ring.
No carcinogenicity was detected with parsley apiol or dill apiol in mice.
- Azeez, Shamina (2008). Chemistry of Spices. Calicut, Kerala, India: Biddles Ltd. pp. 227–241 . 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. 5 (12). pp. 1623–8.
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