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4-phenyl-9H-fluoren-9-one is an organic compound with the molecular formula C20H14O and a molecular weight of 270.32 g/mol. It is a derivative of fluorenone, featuring a phenyl group attached to the 4-position of the fluorenone core. This white crystalline solid is characterized by its melting point of 195-197°C and is soluble in organic solvents such as ethanol and acetone. The compound is synthesized through various methods, including the Friedel-Crafts acylation of fluorene with benzoyl chloride. 4-phenyl-9H-fluoren-9-one is utilized in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It is also employed as a building block in the preparation of advanced materials and dyes.

4269-14-1

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4269-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4269-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4269-14:
(6*4)+(5*2)+(4*6)+(3*9)+(2*1)+(1*4)=91
91 % 10 = 1
So 4269-14-1 is a valid CAS Registry Number.

4269-14-1Downstream Products

4269-14-1Relevant academic research and scientific papers

Spirobifluorene Regioisomerism: A Structure–Property Relationship Study

Sicard, Lambert,Quinton, Cassandre,Peltier, Jean-David,Tondelier, Denis,Geffroy, Bernard,Biapo, Urelle,Métivier, Rémi,Jeannin, Olivier,Rault-Berthelot, Jo?lle,Poriel, Cyril

supporting information, p. 7719 - 7727 (2017/06/06)

The present works report the first structure–property relationship study of a key class of organic semiconductors, that is, the four spirobifluorene positional isomers possessing a para-, meta- or ortho-linkage. The remarkable and surprising impact of the ring bridging and of the linkages on the electronic properties of the regioisomers has been particularly highlighted and rationalised. The impact of the ring bridging on the photophysical properties has been stressed with notably the different influence of the linkages and the bridge on the singlet and triplet excited states. The first member of a new family of spirobifluorenes substituted in the 1-position, which presents better performance in blue phosphorescent OLEDs than those of its regioisomers, is reported. These features highlight not only the great potential of 1-substituted spirobifluorenes, but also the remarkable impact of regioisomerism on electronic properties.

Aluminum oxide mediated C-F bond activation in trifluoromethylated arenes

Papaianina,Amsharov

, p. 1505 - 1508 (2016/01/25)

Thermally activated γ-aluminium oxide was found to be very effective for C-F bond activation in trifluoromethylated arenes. Depending on the activation degree the respective arenes can be converted either to cyclic ketones or to the respective carboxylic acids with good to excellent yields.

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