I2002
1,3-Indandione
97%
Synonym(s):
1,3-Dioxoindan
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About This Item
Empirical Formula (Hill Notation):
C9H6O2
CAS Number:
Molecular Weight:
146.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-109-7
Beilstein/REAXYS Number:
1210061
MDL number:
Assay:
97%
InChI key
UHKAJLSKXBADFT-UHFFFAOYSA-N
InChI
1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2
SMILES string
O=C1CC(=O)c2ccccc12
assay
97%
mp
129-132 °C (lit.)
Quality Level
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Halise Inci Gul et al.
Anti-cancer agents in medicinal chemistry, 18(12), 1770-1778 (2018-05-26)
In this study, new azafluorenones, 4-(4-fluorophenyl)-2-(4-substitutedphenyl)-5Hindeno[ 1,2-b] pyridin-5-one, I1-I8 were synthesized and chemical structures were elucidated by spectral analysis. All compounds were reported for the first time here. Compounds were tested in terms of cytotoxicity. They were found as cytotoxins/anticancer
V Violet Dhayabaran et al.
Journal of fluorescence, 27(1), 135-150 (2016-10-04)
Novel bioactive complexes of Co(II), Cu(II), Ni(II) and Zn(II) metal ions with Schiff base ligand derived from histidine and 1,3-indandione were synthesized and thoroughly characterized by various analytical and spectral techniques. The biological investigations were carried out to examine the
[Effect of S-oxidation on the anticoagulant effects of 4-hydroxycoumarins, 4-hydroxy-2-pyrones and 1,3-indanediones].
K Rehse et al.
Archiv der Pharmazie, 317(3), 262-267 (1984-03-01)
Majid M Heravi et al.
Molecular diversity, 13(3), 385-387 (2009-03-03)
Aldehydes, 1,3-indandione and cyclohexylisocyanide undergo smooth coupling-cyclization in water to produce the corresponding 2-(cyclohexylamino)-3-aryl- indeno [1,2-b] furan-4-ones in good yields. Water was used as a solvent to avoid the use of other highly toxic and environmentally unfavorable solvents for this
Bilquees Bano et al.
Bioorganic chemistry, 81, 658-671 (2018-09-27)
Current study deals with the evaluation of indane-1,3-dione based compounds as new class of urease inhibitors. For that purpose, benzylidine indane-1,3-diones (1-30) were synthesized and fully characterized by different spectroscopic techniques including EI-MS, HREI-MS, 1H, and 13C NMR. All synthetic
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