511544
5-Hydroxy-1-indanone
95%
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About This Item
Empirical Formula (Hill Notation):
C9H8O2
CAS Number:
Molecular Weight:
148.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
Product Name
5-Hydroxy-1-indanone, 95%
InChI
1S/C9H8O2/c10-7-2-3-8-6(5-7)1-4-9(8)11/h2-3,5,10H,1,4H2
SMILES string
Oc1ccc2C(=O)CCc2c1
InChI key
ZRKQOVXGDIZYDS-UHFFFAOYSA-N
assay
95%
impurities
<3% acetone
mp
175 °C (dec.) (lit.)
functional group
ketone
Quality Level
Related Categories
Application
5-Hydroxy-1-indanone may be used in the preparation of (5-hydroxy-indan-(1E)-ylidene)-acetic acid and 5-[2-(phenyl)ethoxy]-1-indanone. It may be used as a starting material in the multi-step synthesis of 5H-indeno[1,2-c]pyridazin-5-one analogs.
General description
5-Hydroxy-1-indanone is a 1-indanone derivative.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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On the involvement of single-bond rotation in the primary photochemistry of photoactive yellow protein.
Stahl AD, et al.
Biophysical Journal, 101(5), 1184-1192 (2011)
Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,p* and p,p* triplets.
Lathioor EC and Leigh WJ.
Canadian Journal of Chemistry, 79(12), 1851-1863 (2001)
J Reniers et al.
European journal of medicinal chemistry, 46(12), 6104-6111 (2011-10-25)
Previous studies on 5H-indeno[1,2-c]pyridazin-5-one derivatives as inhibitors of MAO-B revealed that it was possible to increase the MAO-B inhibitory potency of 5H-indeno[1,2-c]pyridazin-5-ones by substituting the central heterocycle in the 3-position or C-8 with lipophilic groups which occupy the substrate cavity
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