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Merck
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Key Documents

Otros documentos

I2002

Sigma-Aldrich

1,3-Indandione

97%

Sinónimos:

1,3-Dioxoindan

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About This Item

Fórmula empírica (notación de Hill):
C9H6O2
Número de CAS:
606-23-5
Peso molecular:
146.14
Beilstein/REAXYS Number:
1210061
EC Number:
210-109-7
MDL number:
MFCD00003779
UNSPSC Code:
12352100
PubChem Substance ID:
24895958
NACRES:
NA.22

assay

97%

mp

129-132 °C (lit.)

SMILES string

O=C1CC(=O)c2ccccc12

InChI

1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2

InChI key

UHKAJLSKXBADFT-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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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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