Home › Entities › type_of_chemical_entity › 3-methylbut-2-en-1-ol

3-methylbut-2-en-1-ol

chemical compound
ChemicalSubstance type_of_chemical_entity Q425512
Press Enter · cited answer in seconds

3-methylbut-2-en-1-ol

Summary

3-methylbut-2-en-1-ol is a type of chemical entity[1]. 3-methylbut-2-en-1-ol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • 3-methylbut-2-en-1-ol's instance of is recorded as type of chemical entity[3].
  • 3-methylbut-2-en-1-ol's CAS Registry Number is recorded as 556-82-1[4].
  • 3-methylbut-2-en-1-ol's EC number is recorded as 209-141-4[5].
  • 3-methylbut-2-en-1-ol's canonical SMILES is recorded as CC(=CCO)C[6].
  • 3-methylbut-2-en-1-ol's InChI is recorded as InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3[7].
  • 3-methylbut-2-en-1-ol's InChIKey is recorded as ASUAYTHWZCLXAN-UHFFFAOYSA-N[8].
  • 3-methylbut-2-en-1-ol's chemical formula is recorded as C₅H₁₀O[9].
  • 3-methylbut-2-en-1-ol's subclass of is recorded as fatty alcohol[10].
  • 3-methylbut-2-en-1-ol's subclass of is recorded as alkenol[11].
  • 3-methylbut-2-en-1-ol's part of is recorded as prenol metabolic process[12].
  • 3-methylbut-2-en-1-ol's part of is recorded as prenol biosynthetic process[13].
  • 3-methylbut-2-en-1-ol's part of is recorded as prenol catabolic process[14].
  • 3-methylbut-2-en-1-ol's part of is recorded as prenyl-diphosphatase activity[15].
  • 3-methylbut-2-en-1-ol's Commons category is recorded as Prenol[16].
  • 3-methylbut-2-en-1-ol's ChEMBL ID is recorded as CHEMBL3184952[17].
  • 3-methylbut-2-en-1-ol's Freebase ID is recorded as /m/09d5bs[18].
  • 3-methylbut-2-en-1-ol's UNII is recorded as 55MY0HM445[19].
  • 3-methylbut-2-en-1-ol's ChemSpider ID is recorded as 10700[20].
  • 3-methylbut-2-en-1-ol's PubChem CID is recorded as 11173[21].
  • 3-methylbut-2-en-1-ol's KEGG ID is recorded as C17628[22].
  • 3-methylbut-2-en-1-ol's ZVG number is recorded as 493271[23].
  • 3-methylbut-2-en-1-ol's ChEBI ID is recorded as 16019[24].
  • 3-methylbut-2-en-1-ol's found in taxon is recorded as Coffea arabica[25].
  • 3-methylbut-2-en-1-ol's found in taxon is recorded as Opuntia ficus-indica[26].
  • 3-methylbut-2-en-1-ol's found in taxon is recorded as Alpinia officinarum[27].

Why It Matters

3-methylbut-2-en-1-ol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] 3-methylbut-2-en-1-ol has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] 3-methylbut-2-en-1-ol is known by 26 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  13. [15] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEMBL. Retrieved . wikidata.org.
  16. [18] ↑ . Freebase Data Dumps. wikidata.org.
  17. [19] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  18. [20] ↑ . Q2311683. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . ChEBI. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . ChEMBL. Retrieved . wikidata.org.
  23. [25] ↑ . New volatile components of roasted coffee. wikidata.org.
  24. [26] ↑ . Volatile constituents of prickly pear (Opuntia ficus indica Mill., de Castilla variety). wikidata.org.
  25. [27] ↑ . Isolation and structural elucidation of some glycosides from the rhizomes of smaller galanga (Alpinia officinarum Hance).. 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). 3-methylbut-2-en-1-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-methylbut-2-en-1-ol
MLA “3-methylbut-2-en-1-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-methylbut-2-en-1-ol.
BibTeX @misc{4ortxyz_3-methylbut-2-en-1-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3-methylbut-2-en-1-ol}}, year = {2026}, url = {https://4ort.xyz/entity/3-methylbut-2-en-1-ol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3-methylbut-2-en-1-ol — https://4ort.xyz/entity/3-methylbut-2-en-1-ol (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/3-methylbut-2-en-1-ol · Last refreshed: