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dillapiole

chemical compound
Class type of: chemical compound Q419537

Facts

7 properties
Instance of
type of chemical entity
Subclass of
chemical compound
Canonical SMILES
COC1=C(C2=C(C=C1CC=C)OCO2)OC[5]
Chemical formula
C₁₂H₁₄O₄[6]
Found in taxon
Crithmum maritimum, Peperomia pellucida, Aniba ferrea, Pimpinella serbica, Piper marginatum, Anethum graveolens, Brucea javanica, Coriandrum sativum, Peucedanum zenkeri, Perilla frutescens, Protium heptaphyllum, West African Pepper, Foeniculum vulgare, Piper regnellii, Piper solmsianum, Endlicheria, Piper pedicellosum, Ocotea aciphylla, Piper auritum, Licaria canella, Heterotropa, Perilla frutescens var. crispa, Codonopsis cordifolioidea, Ligusticum scothicum, Piper aduncum, Mangifera indica, Carum montanum, Apium graveolens, Heterotropa, Piper neesii, Asarum yaeyamense, Mespilodaphne cymbarum[7][8][9][10][11][12][13][14][15][16][17][18][19][20]
Mass
+222.089[21]
Named after
Anethum graveolens, apiole[3][4]
🏷️ Also known as
en 4,5-Dimethoxy-6-(2-propenyl)-1,3-benzodioxole en dillapiol en dillapiole ar ديلابيول fa دیلاپیول fi tilliapioli id Dilapiola it dillapiolo ja ジラピオール pt dilapiol
🔖 Identifiers · 19
CAS Registry Number
484-31-1
ChEBI ID
70453
ChEMBL ID
CHEMBL470874
ChemSpider ID
9814
DSSTox substance ID
DTXSID80862007
EC number
621-020-1
ECHA Substance Infocard ID
100.149.911
Freebase ID
/m/0267mt8
Human Metabolome Database ID
HMDB0030725
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
InChIKey
LIKYNOPXHGPMIH-UHFFFAOYSA-N
KEGG ID
C10449
Show all 19 identifiers +7
KNApSAcK ID
C00002737
Microsoft Academic ID (discontinued)
2777651005
PubChem CID
10231
SPLASH
splash10-00di-9660000000-7cd909d21ca4a4c8bb1e
SureChEMBL ID
310992
UNII
438CJQ562D
UniChem compound ID
315361

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🔗 Connections
Found in taxon 22
Coriandrum sativum, Foeniculum vulgare, Anethum graveolens, Mangifera indica, Apium graveolens, Crithmum maritimum, Perilla frutescens, Peperomia pellucida +14 more
Named after 2
Anethum graveolens, apiole
Subclass of 1
chemical compound
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Summary

dillapiole is a type of chemical entity[1]. dillapiole is a type of chemical compound[2].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [2] ↑ . wikidata.org.
  6. [7] ↑ . Composition and antibacterial activity of the essential oil fromCrithmum maritimum L. (Apiaceae) growing wild in Turkey. wikidata.org.
  7. [8] ↑ . The essential oils ofPeperomia pellucida Kunth andP. circinnata Link var.circinnata. wikidata.org.
  8. [9] ↑ . Neolignans from Aniba ferrea. wikidata.org.
  9. [10] ↑ . Essential Oil from Pimpinella serbica Fruits. wikidata.org.
  10. [11] ↑ . Essential Oil of Piper marginatum. wikidata.org.
  11. [12] ↑ . Effect of Ascorbic Acid on the Yield and Quality of Essential Oils in Indian Dark Variyali Sowa (Anethum sowa). wikidata.org.
  12. [13] ↑ . A New Monoterpene Lactone and Chemical Composition of Essential Oil ofBrucea jawanicaLeaves. wikidata.org.
  13. [14] ↑ . Chemical Composition of the Seed Oil ofCoriandrum sativumL. from Cuba. wikidata.org.
  14. [15] ↑ . Aromatic Plants of Tropical Central Africa. XVIII. Essential Oils of Leaf and Rhizome ofPeucedanum zenkeriEngl. from Cameroon. wikidata.org.
  15. [16] ↑ . Genetic control of the chemical composition of volatile oils in Perilla frutescens. wikidata.org.
  16. [17] ↑ . Volatile Constituents from Leaves and Stems ofProtium heptaphyllum(Aubl.) March.. wikidata.org.
  17. [18] ↑ . Essential oil constituents of Ashanti pepper (Piper guineense) fruits (berries). wikidata.org.
  18. [19] ↑ . Antimicrobial constituents of Foeniculum vulgare. wikidata.org.
  19. [20] ↑ . Phenylpropanoids and neolignans from Piper regnellii. wikidata.org.
  20. [21] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). dillapiole. Retrieved November 7, 2026, from https://4ort.xyz/entity/dillapiole
MLA “dillapiole.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/dillapiole.
BibTeX @misc{4ortxyz_dillapiole_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dillapiole}}, year = {2026}, url = {https://4ort.xyz/entity/dillapiole}, note = {Accessed: 2026-11-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): dillapiole — https://4ort.xyz/entity/dillapiole (retrieved 2026-11-07)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of → type of chemical entity
    Named after → Anethum graveolens, apiole
    Found in taxon → Crithmum maritimum, Peperomia pellucida, Aniba ferrea +29
    Subclass of → chemical compound
    + 1 other property edited (see Wikidata diff for full list)
    "Changed [tr] labels, descriptions or aliases: QuickStatements 3.0 batch #37300"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.