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2-acetylfuran

chemical compound
Class type of: chemical compound Q15634156

Facts

7 properties
Instance of
type of chemical entity
Subclass of
chemical compound[4]
Canonical SMILES
CC(=O)C1=CC=CO1[2]
Chemical formula
C₆H₆O₂[3]
Found in taxon
Coffea arabica, Psidium guajava, Asarum canadense, Campsis grandiflora, Castanopsis cuspidata, liquorice, Mangifera indica, Polygala senega, Tamarindus indica, Theobroma cacao, Vaccinium ashei, Vitis rotundifolia, Akebia trifoliata, Panax ginseng, Terminalia chebula, maize, Vaccinium virgatum, Vaccinium corymbosum, Capparis spinosa[5][6][7][8][9][10][11][12][13][14][15][16][17][18]
Mass
+110.037[19]
Melting point
+29[20]
🏷️ Also known as
en Furyl methyl ketone en Ketone, 2-furyl methyl en Methyl 2-furyl ketone en 1-(2-furanyl)ethanone en 1-(2-Furanyl)-ethanone en 1-(2-Furanyl)-ethanone (2-acetylfuran) en 1-(2-Furanyl)ethanone, 9CI en 1-(2-Furanyl)ethanone (acetylfuran) en 1-(2-Furyl)ethanone en 1-(furan-2-yl)ethan-1-one en 1-(Furan-2-yl)ethanone en 2-Acetofurone en 2-acetylfuran en 2-Acetyl-Furan en 2-Acetylfurane en (2-furanyl)-1-ethanone en 2-Furylethanone en 2-Furyl methyl ketone en Acetylfuran en a-Furyl methyl ketone
🔖 Identifiers · 31
CAS Registry Number
1192-62-7
Cannabis Database ID
005818
ChEBI ID
59983
ChemSpider ID
13849
CosIng number
40013
DSSTOX compound identifier
DTXCID1030153
DSSTox substance ID
DTXSID0051601
EC number
214-757-1
ECHA Substance Infocard ID
100.013.416
FL number
13.054
Freebase ID
/m/0zbyc36
Gmelin number
50073
Show all 31 identifiers +19
Human Metabolome Database ID
HMDB0033127
IEDB Epitope ID
136039
InChI
InChI=1S/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H3
InChIKey
IEMMBWWQXVXBEU-UHFFFAOYSA-N
JECFA number
1503
KNApSAcK ID
C00029371
MassBank accession ID
MSBNK-Fac_Eng_Univ_Tokyo-JP006946, MSBNK-Fac_Eng_Univ_Tokyo-JP007735
Microsoft Academic ID (discontinued)
2776329038
NMRShiftDB structure ID
10017951
NSC number
4665, 49133
Probes And Drugs ID
PD158331
PubChem CID
14505
Reaxys registry number
107909
SPLASH
splash10-01ow-9200000000-39cadbe5f909cbb066e3, splash10-0002-9200000000-02caa47cd67aaabc5a45
ScienceDirect topic ID
chemistry/2-acetylfuran
SureChEMBL ID
43960
UNII
Q5ZRP80K02
UniChem compound ID
1100477
ZVG number
493943

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Found in taxon 18
maize, Tamarindus indica, Theobroma cacao, liquorice, Mangifera indica, Psidium guajava, Capparis spinosa, Coffea arabica +10 more
Subclass of 1
chemical compound
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Summary

2-acetylfuran is a type of chemical entity[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . New volatile components of roasted coffee. wikidata.org.
  5. [6] ↑ . Volatile flavour components of guava. wikidata.org.
  6. [7] ↑ . Composition of the essential oil from Asarum canadense. wikidata.org.
  7. [8] ↑ . The essential oil from the flowers ofCampsis grandiflora (Thumb.) K. Schum. from China. wikidata.org.
  8. [9] ↑ . Volatile constituents of Castanopsis flower. wikidata.org.
  9. [10] ↑ . Volatile flavor components of licorice. wikidata.org.
  10. [11] ↑ . Volatile aroma constituents of mango (cv Kensington). wikidata.org.
  11. [12] ↑ . Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots. wikidata.org.
  12. [13] ↑ . Volatile Flavor Components of Tamarind (Tamarindus indicaL.). wikidata.org.
  13. [14] ↑ . Steam volatile aroma constituents of roasted cocoa beans. wikidata.org.
  14. [15] ↑ . Comparison of the Volatile Constituents from Rabbiteye Blueberries (Vaccinium ashei) During Ripening. wikidata.org.
  15. [16] ↑ . Identification of the Volatile Constituents from Scuppernong Berries (Vitis rotundifolia). wikidata.org.
  16. [17] ↑ . Constituents of essential oil from the dried fruits and stems of Akebia quinata (THUNB.) DECNE.. wikidata.org.
  17. [18] ↑ . Determination of volatile organic compounds generated from fresh, white and red Panax ginseng (C. A. Meyer) using a direct sample injection technique. wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . Jean-Claude Bradley Open Melting Point Dataset. 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). 2-acetylfuran. Retrieved November 6, 2026, from https://4ort.xyz/entity/2-acetylfuran
MLA “2-acetylfuran.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/2-acetylfuran.
BibTeX @misc{4ortxyz_2-acetylfuran_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-acetylfuran}}, year = {2026}, url = {https://4ort.xyz/entity/2-acetylfuran}, note = {Accessed: 2026-11-06}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 2-acetylfuran — https://4ort.xyz/entity/2-acetylfuran (retrieved 2026-11-06)

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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. 26w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Subclass of → chemical compound
    Melting point → 29 degree Celsius
    Instance of → type of chemical entity
    Mass → 110.037 dalton
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.