sinapyl alcohol

chemical compound
ChemicalSubstance type_of_chemical_entity Q418975
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sinapyl alcohol

Summary

sinapyl alcohol is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • sinapyl alcohol's instance of is recorded as type of chemical entity[3].
  • sinapyl alcohol's chemical structure is recorded as Sinapyl alcohol.svg[4].
  • sinapyl alcohol's CAS Registry Number is recorded as 537-33-7[5].
  • sinapyl alcohol's EC number is recorded as 664-272-8[6].
  • sinapyl alcohol's canonical SMILES is recorded as COC1=CC(=CC(=C1O)OC)C=CCO[7].
  • sinapyl alcohol's InChI is recorded as InChI=1S/C11H14O4/c1-14-9-6-8(4-3-5-12)7-10(15-2)11(9)13/h3-4,6-7,12-13H,5H2,1-2H3/b4-3+[8].
  • sinapyl alcohol's InChIKey is recorded as LZFOPEXOUVTGJS-ONEGZZNKSA-N[9].
  • sinapyl alcohol's chemical formula is recorded as C₁₁H₁₄O₄[10].
  • sinapyl alcohol's subclass of is recorded as sinapic alcohol[11].
  • sinapyl alcohol's part of is recorded as sinapyl alcohol dehydrogenase activity[12].
  • sinapyl alcohol's Commons category is recorded as Sinapyl alcohol[13].
  • sinapyl alcohol's ChEMBL ID is recorded as CHEMBL1800816[14].
  • sinapyl alcohol's PDB structure ID is recorded as 5CVU[15].
  • sinapyl alcohol's Freebase ID is recorded as /m/0f9n7n[16].
  • sinapyl alcohol's UNII is recorded as 8O6NO04SMV[17].
  • sinapyl alcohol's ChemSpider ID is recorded as 4444145[18].
  • sinapyl alcohol's PubChem CID is recorded as 5280507[19].
  • sinapyl alcohol's KEGG ID is recorded as C02325[20].
  • sinapyl alcohol's ChEBI ID is recorded as 64557[21].
  • sinapyl alcohol's found in taxon is recorded as Tabernaemontana divaricata[22].
  • sinapyl alcohol's found in taxon is recorded as Fagus grandifolia[23].
  • sinapyl alcohol's found in taxon is recorded as Pisum sativum[24].
  • sinapyl alcohol's found in taxon is recorded as Saccharum officinarum[25].
  • sinapyl alcohol's found in taxon is recorded as Streptomyces nigra[26].
  • sinapyl alcohol's found in taxon is recorded as Aeschynanthus bracteatus[27].

Why It Matters

sinapyl alcohol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] It is known by 7 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 . wikidata.org.
  4. [6] . ECHA Substance Infocard database. 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] . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . Protein Data Bank. Retrieved . wikidata.org.
  14. [16] . Freebase Data Dumps. wikidata.org.
  15. [17] . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] . Q2311683. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . ChEBI. Retrieved . wikidata.org.
  19. [21] . ChEMBL. Retrieved . wikidata.org.
  20. [22] . Capillary Gas Chromatographic Analysis of Indole Alkaloids: Investigation of the Indole Alkaloids Present in Tabernaemontana divaricata Cell Suspension Culture. wikidata.org.
  21. [23] . Cis-monolignols in Fagus grandifolia and their possible involvement in lignification. wikidata.org.
  22. [24] . Identification of Plant Factors Inducing Virulence Gene Expression in Agrobacterium tumefaciens.. wikidata.org.
  23. [25] . Antioxidative Compounds Isolated from Kokuto, Non-centrifugal Cane Sugar. wikidata.org.
  24. [26] . Streptomyces nigra sp. nov. Is a Novel Actinobacterium Isolated From Mangrove Soil and Exerts a Potent Antitumor Activity in Vitro. wikidata.org.
  25. [27] . Chemical constituents of Aeschynanthus bracteatus and their weak anti-inflammatory activities.. 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). sinapyl alcohol. Retrieved May 3, 2026, from https://4ort.xyz/entity/sinapyl-alcohol
MLA “sinapyl alcohol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sinapyl-alcohol.
BibTeX @misc{4ortxyz_sinapyl-alcohol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{sinapyl alcohol}}, year = {2026}, url = {https://4ort.xyz/entity/sinapyl-alcohol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): sinapyl alcohol — https://4ort.xyz/entity/sinapyl-alcohol (retrieved 2026-05-03)

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