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Anthracen-1-yl(phenyl)methanone, also known as 9-phenyl-9-anthracenone or 9-phenyl-9H-fluorenone, is an organic compound with the chemical formula C21H14O. It is a derivative of anthracene, a tricyclic aromatic hydrocarbon, and phenyl, a benzene ring. anthracen-1-yl(phenyl)methanone is characterized by the presence of a ketone functional group (C=O) and exhibits a planar structure due to the conjugation between the anthracene and phenyl rings. Anthracen-1-yl(phenyl)methanone is a white crystalline solid with a melting point of around 180°C. It is used in the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries, and has potential applications in the development of dyes, pigments, and other specialty chemicals.

1564-52-9

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1564-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1564-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1564-52:
(6*1)+(5*5)+(4*6)+(3*4)+(2*5)+(1*2)=79
79 % 10 = 9
So 1564-52-9 is a valid CAS Registry Number.

1564-52-9Downstream Products

1564-52-9Relevant academic research and scientific papers

Synthesis of hierarchical Beta using piperidine based multi-ammonium surfactants

Kore, Rajkumar,Sridharkrishna,Srivastava, Rajendra

, p. 1317 - 1322 (2013/03/14)

Hierarchical Beta zeolite was prepared using piperidine based structure directing agents having at least two ammonium groups in their structure. Materials exhibited very high surface area (≈1050 m2 g -1), pore volume (2.7 mL g-1), and catalytic activity hitherto reported in the literature. A density functional theoretical study shows that a suitable special orientation of piperidine rings in the structure directing agents is responsible for the formation of hierarchical Beta.

SOME RELATIONSHIPS GOVERNING THE DEACYLATION OF SUBSTITUTED 9-BENZOYLANTHRACENES

Bokova, A. I.,Buchina, I. K.

, p. 1199 - 1201 (2007/10/02)

In the presence of small amounts of ferric chloride substituted 9-benzoylanthracenes are deacylated, isomerized, and reacylated.The degree of transformation of the ketones increases with increase in the effective volume of the substituent at the ortho position to the acyl and with increase in the electron-donating characteristics of the substituent in the aromatic rings.

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