1-methylcyclopropene

synthetic plant growth regulator blocking the effects of ethylene (competitive inhibitor)
ChemicalSubstance type_of_chemical_entity Q161651
Press Enter · cited answer in seconds

1-methylcyclopropene

Summary

1-methylcyclopropene is a type of chemical entity[1]. 1-methylcyclopropene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (38 views/month).[2]

Key Facts

  • 1-methylcyclopropene's instance of is recorded as type of chemical entity[3].
  • 1-methylcyclopropene's chemical structure is recorded as 1-methylcycloprop-1-ene 200.svg[4].
  • 1-methylcyclopropene's CAS Registry Number is recorded as 3100-04-7[5].
  • 1-methylcyclopropene's EC number is recorded as 608-567-1[6].
  • 1-methylcyclopropene's canonical SMILES is recorded as CC1=CC1[7].
  • 1-methylcyclopropene's InChI is recorded as InChI=1S/C4H6/c1-4-2-3-4/h2H,3H2,1H3[8].
  • 1-methylcyclopropene's InChIKey is recorded as SHDPRTQPPWIEJG-UHFFFAOYSA-N[9].
  • 1-methylcyclopropene's chemical formula is recorded as C₄H₆[10].
  • 1-methylcyclopropene's subclass of is recorded as cycloalkene[11].
  • 1-methylcyclopropene's Commons category is recorded as 1-Methylcyclopropene[12].
  • 1-methylcyclopropene's MeSH descriptor ID is recorded as C412563[13].
  • 1-methylcyclopropene's has part is recorded as carbon[14].
  • 1-methylcyclopropene's has part is recorded as hydrogen[15].
  • 1-methylcyclopropene's Freebase ID is recorded as /m/03mh9wc[16].
  • 1-methylcyclopropene's UNII is recorded as J6UJO23JGU[17].
  • 1-methylcyclopropene's ChemSpider ID is recorded as 133162[18].
  • 1-methylcyclopropene's PubChem CID is recorded as 151080[19].
  • 1-methylcyclopropene's ChEBI ID is recorded as 132592[20].
  • 1-methylcyclopropene's found in taxon is recorded as Prunus avium[21].
  • 1-methylcyclopropene's Reaxys registry number is recorded as 635679[22].
  • 1-methylcyclopropene's NALT ID is recorded as 153511[23].
  • 1-methylcyclopropene's HSDB ID is recorded as 7517[24].
  • 1-methylcyclopropene's KNApSAcK ID is recorded as C00058851[25].
  • 1-methylcyclopropene's mass is recorded as {'unit': 'Q483261', 'amount': '+54.047'}[26].
  • 1-methylcyclopropene's melting point is recorded as {'unit': 'Q25267', 'amount': '+100'}[27].

Why It Matters

1-methylcyclopropene ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (38 views/month).[2] 1-methylcyclopropene has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[28] 1-methylcyclopropene is known by 5 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] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: 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] . wikidata.org.
  11. [13] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . 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] . Postharvest responses of sweet cherry fruit and stem tissues revealed by metabolomic profiling. wikidata.org.
  20. [22] . ChEBI. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . Hazardous Substances Data Bank. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . bvl.bund.de. Retrieved . bvl.bund.de. Provenance: 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). 1-methylcyclopropene. Retrieved May 3, 2026, from https://4ort.xyz/entity/1-methylcyclopropene
MLA “1-methylcyclopropene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/1-methylcyclopropene.
BibTeX @misc{4ortxyz_1-methylcyclopropene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{1-methylcyclopropene}}, year = {2026}, url = {https://4ort.xyz/entity/1-methylcyclopropene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 1-methylcyclopropene — https://4ort.xyz/entity/1-methylcyclopropene (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/1-methylcyclopropene · Last refreshed: