Indenol

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For trade name of a drug, see Propranolol.
Indenol

Chemical structure of 1-indenol
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 1-ol: 260-294-3
  • 1-ol: InChI=1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-6,9-10H
    Key: KWRSKZMCJVFUGU-UHFFFAOYSA-N
  • 1-ol: C1=CC=C2C(C=CC2=C1)O
Properties
C9H8O
Molar mass 132.162 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Indenols are hydroxylated indene. 3-Indenol is an enol forms of 1-indanone, and 2-indenol is an enol form of 2-indanone. Isomerization of 1-indenol can produce 1-indanone.[1] Indenolol is a derivative of a phenolic indenol.[2]

References

  1. ^ Connors N, Prevoznak R, Chartrain M, Reddy J, Singhvi R, Patel Z, et al. (1997). "Conversion of indene to cis -(1 S ),(2 R )-indandiol by mutants of Pseudomonas putida F1". Journal of Industrial Microbiology and Biotechnology. 18 (6): 353–359. doi:10.1038/sj.jim.2900402. S2CID 37645524.
  2. ^ Trimarco B, Cuocolo A, Groothold G, Ricciardelli B, De Luca N, Volpe M, et al. (1985). "Indenolol: a new antihypertensive agent: efficacy, toxicity, and hemodynamic effects in a crossover double-blind study with metoprolol". Journal of Clinical Pharmacology. 25 (5): 328–36. doi:10.1002/j.1552-4604.1985.tb02850.x. PMID 4031109. S2CID 22844379.
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