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1-nitro-9H-fluoren-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56825-82-2

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56825-82-2 Usage

Physical form

Yellow crystalline solid

Usage

Pharmaceutical and organic synthesis, precursor in the production of fluorescent materials and dyes

Pharmaceutical applications

Potential development of anti-cancer drugs

Environmental impact

Potential pollutant, harmful if ingested, inhaled, or absorbed through the skin, poses health risks to humans and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 56825-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56825-82:
(7*5)+(6*6)+(5*8)+(4*2)+(3*5)+(2*8)+(1*2)=152
152 % 10 = 2
So 56825-82-2 is a valid CAS Registry Number.

56825-82-2Downstream Products

56825-82-2Relevant academic research and scientific papers

Synthesis of fluorenones via quaternary ammonium salt-promoted intramolecular dehydrogenative arylation of aldehydes

Shi, Zhuangzhi,Glorius, Frank

, p. 829 - 833 (2013/03/28)

Biologically interesting fluorenone, xanthone and anthrone derivatives have been prepared via an intramolecular oxidative acylation process. This novel direct acylation reaction proceeded without the aid of any transition metals, acids or bases, and uses a catalytic amount of a quaternary ammonium salt in the presence of a persulfate oxidant. Initial mechanistic studies have been carried out to elucidate the reaction pathway. The Royal Society of Chemistry 2013.

Decarboxylative C-H arylation of benzoic acids under radical conditions

Seo, Sangwon,Slater, Mark,Greaney, Michael F.

supporting information; experimental part, p. 2650 - 2653 (2012/07/27)

A decarboxylative radical cyclization reaction has been developed for the synthesis of fluorenones. The reaction uses Ag(I)/K2S 2O8 to oxidatively decarboxylate an aroylbenzoic acid to an aryl radical, which undergoes cyclization to afford fluorenone products in good yield.

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