Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C10H18O2
- Molecular weight
- 170.25 g/mol
- IUPAC name
- (1S)-5-(2-hydroxypropan-2-yl)-2-methylcyclohex-2-en-1-ol
via PubChem
Research
77 papers- Sobrerol: New Perspectives to Manage Patients with Frequent Respiratory Infections.Children (Basel, Switzerland) · 2023
- Sobrerol in Managing Acute Respiratory Infections in Clinical Practice During the "Cold" Season: An Italian Primary Care Experience.International journal of general medicine · 2024
- Sobrerol Improves Memory Impairment in the Scopolamine-Induced Amnesia Mouse Model.International journal of molecular sciences · 2025
- [Carbocysteine-sobrerol combination and exacerbation of chronic bronchitis].Archivio Monaldi per le malattie del torace · 1988
- Sobrerol in the treatment of secretory otitis media in childhood.The Journal of international medical research · 1989
via PubMed
Wikidata facts
- Mass
- 170.13068
Show 4 more facts
- chemical formula
- C₁₀H₁₈O₂
- isomeric SMILES
- CC1=CCC(C[C@@H]1O)C(C)(C)O
- canonical SMILES
- CC1=CCC(CC1O)C(C)(C)O
- Commons category
- Sobrerol
Sources (1)
via Wikidata · CC0
~1 min read
Article
2 sectionsContents
- History
- References
Sobrerol is a mucolytic.
==History== Sobrerol was discovered by Ascanio Sobrero as an oxidation product of terpenes. Later the oxidation and reduction reactions of chiral pinene lead also to several possible isomers of carvone (the corresponding cyclohexyl ketone dehydrated at the isopropyl) and sobrerol, making it possible to determine reaction mechanism and the structural properties of pinene and of other terpenes.
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