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Merck
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Key Documents

Altri documenti

I2002

Sigma-Aldrich

1,3-Indandione

97%

Sinonimo/i:

1,3-Dioxoindan

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About This Item

Formula empirica (notazione di Hill):
C9H6O2
Numero CAS:
606-23-5
Peso molecolare:
146.14
Beilstein:
1210061
Numero CE:
210-109-7
Numero MDL:
MFCD00003779
Codice UNSPSC:
12352100
ID PubChem:
24895958
NACRES:
NA.22

Saggio

97%

Punto di fusione

129-132 °C (lit.)

Stringa SMILE

O=C1CC(=O)c2ccccc12

InChI

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

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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1,3-Cycloheptanedione 97%

Sigma-Aldrich

515981

1,3-Cycloheptanedione

5,5-Dimethyl-1,3-cyclohexanedione 95%

Sigma-Aldrich

D153303

5,5-Dimethyl-1,3-cyclohexanedione

4-Cyclopentene-1,3-dione 95%

Sigma-Aldrich

161683

4-Cyclopentene-1,3-dione

[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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