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4-Nerolidylcatechol

group of stereoisomers with the chemical formula C₂₁H₃₀O₂
ChemicalSubstance group_of_stereoisomers Q105370928
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4-Nerolidylcatechol

Summary

4-Nerolidylcatechol is a group of stereoisomers[1].

Key Facts

  • 4-Nerolidylcatechol's instance of is recorded as group of stereoisomers[2].
  • 4-Nerolidylcatechol's canonical SMILES is recorded as OC1=CC=C(C=C1O)C(C=C)(C)CCC=C(C)CCC=C(C)C[3].
  • 4-Nerolidylcatechol's InChI is recorded as InChI=1S/C21H30O2/c1-6-21(5,18-12-13-19(22)20(23)15-18)14-8-11-17(4)10-7-9-16(2)3/h6,9,11-13,15,22-23H,1,7-8,10,14H2,2-5H3/b17-11+[4].
  • 4-Nerolidylcatechol's InChIKey is recorded as ZBZZDHDWRSFLAY-GZTJUZNOSA-N[5].
  • 4-Nerolidylcatechol's chemical formula is recorded as C₂₁H₃₀O₂[6].
  • 4-Nerolidylcatechol's subclass of is recorded as farnesane sesquiterpenoid[7].
  • 4-Nerolidylcatechol's subclass of is recorded as biogenic alkylphenol[8].
  • 4-Nerolidylcatechol's PubChem CID is recorded as 5352089[9].
  • 4-Nerolidylcatechol's ChEBI ID is recorded as 174288[10].
  • 4-Nerolidylcatechol's found in taxon is recorded as Piper peltatum[11].
  • 4-Nerolidylcatechol's found in taxon is recorded as Piper umbellatum[12].
  • 4-Nerolidylcatechol's isomeric SMILES is recorded as C=CC(C)(CC/C=C(\C)CCC=C(C)C)c1ccc(O)c(O)c1[13].
  • 4-Nerolidylcatechol's Human Metabolome Database ID is recorded as HMDB0031924[14].
  • 4-Nerolidylcatechol's KNApSAcK ID is recorded as C00057535[15].
  • 4-Nerolidylcatechol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+314.2245802'}[16].
  • 4-Nerolidylcatechol's SureChEMBL ID is recorded as 1962024[17].
  • 4-Nerolidylcatechol's UniChem compound ID is recorded as 524449[18].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Investigation of the larvicidal activity of Pothomorphe peltata and isolation of the active constituent. wikidata.org.
  11. [12] ↑ . Biosynthetic origins of the isoprene units of 4-nerolidylcatechol in Potomorphe umbellata. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 4-Nerolidylcatechol. Retrieved May 3, 2026, from https://4ort.xyz/entity/4-nerolidylcatechol
MLA “4-Nerolidylcatechol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/4-nerolidylcatechol.
BibTeX @misc{4ortxyz_4-nerolidylcatechol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{4-Nerolidylcatechol}}, year = {2026}, url = {https://4ort.xyz/entity/4-nerolidylcatechol}, note = {Accessed: 2026-05-03}}
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