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5-(hydroxymethyl)-2-furaldehyde

chemical compound
ChemicalSubstance type_of_chemical_entity Q414606
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5-(hydroxymethyl)-2-furaldehyde

Summary

5-(hydroxymethyl)-2-furaldehyde is a type of chemical entity[1]. 5-(hydroxymethyl)-2-furaldehyde ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (165 views/month).[2]

Key Facts

  • 5-(hydroxymethyl)-2-furaldehyde's instance of is recorded as type of chemical entity[3].
  • 5-(hydroxymethyl)-2-furaldehyde's chemical structure is recorded as Hydroxymethylfurfural-2D-skeletal.png[4].
  • 5-(hydroxymethyl)-2-furaldehyde's CAS Registry Number is recorded as 67-47-0[5].
  • 5-(hydroxymethyl)-2-furaldehyde's EC number is recorded as 200-654-9[6].
  • 5-(hydroxymethyl)-2-furaldehyde's canonical SMILES is recorded as C1=C(OC(=C1)C=O)CO[7].
  • 5-(hydroxymethyl)-2-furaldehyde's InChI is recorded as InChI=1S/C6H6O3/c7-3-5-1-2-6(4-8)9-5/h1-3,8H,4H2[8].
  • 5-(hydroxymethyl)-2-furaldehyde's InChIKey is recorded as NOEGNKMFWQHSLB-UHFFFAOYSA-N[9].
  • 5-(hydroxymethyl)-2-furaldehyde's chemical formula is recorded as C₆H₆O₃[10].
  • 5-(hydroxymethyl)-2-furaldehyde's subclass of is recorded as aldehydes[11].
  • 5-(hydroxymethyl)-2-furaldehyde's Commons category is recorded as Hydroxymethylfurfural[12].
  • 5-(hydroxymethyl)-2-furaldehyde's has part is recorded as oxygen[13].
  • 5-(hydroxymethyl)-2-furaldehyde's has part is recorded as carbon[14].
  • 5-(hydroxymethyl)-2-furaldehyde's ChEMBL ID is recorded as CHEMBL185885[15].
  • 5-(hydroxymethyl)-2-furaldehyde's Guide to Pharmacology Ligand ID is recorded as 10939[16].
  • 5-(hydroxymethyl)-2-furaldehyde's PDB structure ID is recorded as 1QXE[17].
  • 5-(hydroxymethyl)-2-furaldehyde's Freebase ID is recorded as /m/07vp_w[18].
  • 5-(hydroxymethyl)-2-furaldehyde's UNII is recorded as 70ETD81LF0[19].
  • 5-(hydroxymethyl)-2-furaldehyde's RTECS number is recorded as LT7031100[20].
  • 5-(hydroxymethyl)-2-furaldehyde's ChemSpider ID is recorded as 207215[21].
  • 5-(hydroxymethyl)-2-furaldehyde's PubChem CID is recorded as 237332[22].
  • 5-(hydroxymethyl)-2-furaldehyde's KEGG ID is recorded as C11101[23].
  • 5-(hydroxymethyl)-2-furaldehyde's ChEBI ID is recorded as 412516[24].
  • 5-(hydroxymethyl)-2-furaldehyde's found in taxon is recorded as Verruculina enalia[25].
  • 5-(hydroxymethyl)-2-furaldehyde's found in taxon is recorded as Hydrastis canadensis[26].
  • 5-(hydroxymethyl)-2-furaldehyde's found in taxon is recorded as Tropicoporus linteus[27].

Why It Matters

5-(hydroxymethyl)-2-furaldehyde ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (165 views/month).[2] 5-(hydroxymethyl)-2-furaldehyde has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[28] 5-(hydroxymethyl)-2-furaldehyde is known by 29 alternative names across languages and contexts.[29]

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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . ChEMBL. Retrieved . wikidata.org.
  14. [16] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] ↑ . Freebase Data Dumps. wikidata.org.
  17. [19] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . Q2311683. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . ChEMBL. Retrieved . wikidata.org.
  23. [25] ↑ . The metabolites of the mangrove fungus Verruculina enalia No. 2606 from a salt lake in the Bahamas. wikidata.org.
  24. [26] ↑ . Antioxidants in medicinal plant extracts. A research study of the antioxidant capacity of Crataegus, Hamamelis and Hydrastis. wikidata.org.
  25. [27] ↑ . A sphingolipid and tyrosinase inhibitors from the fruiting body of Phellinus linteus. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. 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). 5-(hydroxymethyl)-2-furaldehyde. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-hydroxymethyl-2-furaldehyde
MLA “5-(hydroxymethyl)-2-furaldehyde.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-hydroxymethyl-2-furaldehyde.
BibTeX @misc{4ortxyz_5-hydroxymethyl-2-furaldehyde_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-(hydroxymethyl)-2-furaldehyde}}, year = {2026}, url = {https://4ort.xyz/entity/5-hydroxymethyl-2-furaldehyde}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-(hydroxymethyl)-2-furaldehyde — https://4ort.xyz/entity/5-hydroxymethyl-2-furaldehyde (retrieved 2026-05-03)

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