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2-Anthryldiphenylphosphine is an organophosphorus compound characterized by its unique molecular structure, which consists of a phosphorus atom bonded to two phenyl groups and a 2-anthryl group. The 2-anthryl group is a derivative of anthracene, a three-ring aromatic hydrocarbon, which imparts distinct electronic and steric properties to the molecule. 2-anthryldiphenylphosphine is of interest in the field of organophosphorus chemistry due to its potential applications in various areas, such as in the synthesis of pharmaceuticals, agrochemicals, and materials science. It is also used as a ligand in coordination chemistry, where it can influence the reactivity and selectivity of transition metal complexes. The specific arrangement of the phenyl and anthryl groups around the phosphorus atom gives 2-anthryldiphenylphosphine its characteristic chemical behavior and reactivity, making it a valuable building block in the design of more complex molecules and materials.

1247-92-3

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1247-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1247-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1247-92:
(6*1)+(5*2)+(4*4)+(3*7)+(2*9)+(1*2)=73
73 % 10 = 3
So 1247-92-3 is a valid CAS Registry Number.

1247-92-3Relevant academic research and scientific papers

Synthesis of phosphine oxide-carboxylic acid esters bearing 9,10-dihydro-9,10-ethanoanthracene moiety

Okada, Yoshiharu,Okeya, Kazuhiro,Murata, Yoshiyasu,Aoki, Nakahisa,Aoki, Takahiro,Sugitani, Motoko,Yasui, Satomi,Sawada, Yusuke,Ogura, Fumio

, p. 821 - 829 (2003)

A bulky type of phosphine oxide-carboxylic acid bearing 9,10-dihydro-9,10-ethanoanthracene moiety was synthesized by the Diels-Alder reaction of 2-anthryldiphenylphosphine oxide and methyl acrylate, for which the structure was confirmed on the basis of s

Three colour solid-state luminescence from positional isomers of facilely modified thiophosphoranyl anthracenes

Herbst-Irmer, Regine,Ruth, Paul Niklas,Schillm?ller, Timo,Stalke, Dietmar

supporting information, p. 7479 - 7482 (2020/07/15)

Three positional isomers of thiophosphoranyl anthracene were synthesized and their photophysical properties were investigated. By varying the position of the substituents, blue, green and yellow solid-state fluorescence with differences in the emission wa

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