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I2002

1,3-Indandione

Name: 1,3-Indandione
Brand: ALDRICH

97%

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Synonym(s):

1,3-Dioxoindan

Empirical Formula (Hill Notation):

C₉H₆O₂

CAS Number:

606-23-5

Molecular Weight:

146.14

Beilstein:

1210061

EC Number:

210-109-7

MDL number:

MFCD00003779

PubChem Substance ID:

24895958

NACRES:

NA.22

Quality Level

200

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Synthesis and Cytotoxicities of New Azafluorenones with Apoptotic Mechanism of Action and Cell Cycle Analysis.

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

A green method for the electroorganic synthesis of new 1,3-Indandione derivatives.

Abdolmajid Bayandori Moghaddam et al.

Chemical & pharmaceutical bulletin, 54(10), 1391-1396 (2006-10-04)

This is an environmentally friendly method in the field of electroorganic reactions under controlled potential electrolysis, without toxic reagents at a carbon electrode in an undivided cell which involves the (EC) mechanism reaction and comprises two steps alternatively; (i) electrochemical

Organic synthesis in water: a green protocol for the synthesis of 2-(cyclohexylamino)-3- aryl- indeno[1,2-b]furan-4-ones.

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

Benzylidine indane-1,3-diones: As novel urease inhibitors; synthesis, in vitro, and in silico studies.

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

Hypolipidemic activity of indan-1,3-dione derivatives in rodents.

A R Murthy et al.

Journal of medicinal chemistry, 28(11), 1591-1596 (1985-11-01)

A series of 2-substituted indan-1,3-dione derivatives, including alkyl (C-1-C-5), mono- and disubstituted phenyl, and other 2-aryl derivatives, were tested for hypolipidemic activity of CF1 male mice at 20 mg/kg per day. These derivatives reduced both serum cholesterol and triglycerides after

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