I2002
1,3-Indandione
97%
Sinónimos:
1,3-Dioxoindan
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About This Item
Fórmula empírica (notación de Hill):
C9H6O2
Número de CAS:
Peso molecular:
146.14
Beilstein:
1210061
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
Productos recomendados
Nivel de calidad
Ensayo
97%
mp
129-132 °C (lit.)
cadena SMILES
O=C1CC(=O)c2ccccc12
InChI
1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2
Clave InChI
UHKAJLSKXBADFT-UHFFFAOYSA-N
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Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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[Effect of anticoagulants of the 4-hydroxycoumarin derivative group on aminotransferase activity in vitro and in vivo].
E Marchut et al.
Folia medica Cracoviensia, 22(3-4), 331-339 (1980-01-01)
I H Hall et al.
Anticancer research, 14(5A), 2053-2058 (1994-09-01)
N-Substituted indan-1.3-diones have proven to be potent cytotoxic agents effective against the growth of single cell leukemia tumors and cell lines derived from solid tumors. A number of the derivatives were active against growth of solid tumors e.g. colon, lung
M V Diurno et al.
Bollettino della Societa italiana di biologia sperimentale, 60(1), 79-84 (1984-01-30)
In order to obtain biologically active compounds with a probable anticoagulant activity, some new products, by Michael method from indandione and 2-phenylindandione with ethyl alpha-cyano-beta-aryl-acrylates, have been prepared. The reaction of phenylindandione with methylvinylketone has been also carried out. The
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
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
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