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3-(9-phenanthryl)-1-phenylpropene is an organic compound characterized by a unique molecular structure. It features a phenylpropene backbone, which is a derivative of propene with a phenyl group attached to the third carbon. The distinctive aspect of 3-(9-phenanthryl)-1-phenylpropene is the presence of a 9-phenanthryl group, which is a phenanthrene ring system fused to a benzene ring, attached to the same carbon as the phenyl group. This arrangement endows the molecule with specific optical and electronic properties, making it a subject of interest in the fields of organic chemistry and materials science. The compound's structure contributes to its potential applications in areas such as fluorescence, as a building block in more complex organic syntheses, or in the development of new materials with unique properties.

5751-40-6

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5751-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5751-40-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5751-40:
(6*5)+(5*7)+(4*5)+(3*1)+(2*4)+(1*0)=96
96 % 10 = 6
So 5751-40-6 is a valid CAS Registry Number.

5751-40-6Relevant academic research and scientific papers

Pincer-Nickel-Catalyzed Allyl-Aryl Coupling between Allyl Methyl Ethers and Arylzinc Chlorides

Tao, Jian-Long,Yang, Bo,Wang, Zhong-Xia

, p. 12627 - 12634 (2015)

The P,N,N-pincer nickel complex [Ni(Cl){N(2-Ph2PC6H4)(2′-Me2NC6H4)}]-catalyzed allyl-aryl coupling was studied. The reaction of allyl methyl ethers, including (1-methoxyallyl)arenes and (3-methoxyprop-1-en-1-yl)arenes, with arylzinc chlorides afforded linear (E)-alkenes in high yields, whereas the reaction of (E)-1-methoxytridec-2-ene with p-Me2NC6H4ZnCl generated a mixture of linear and branched alkenes.

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