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α-(9-anthryl)-p-methylbenzyl ethyl ether is a complex organic compound with the molecular formula C23H22O. It is characterized by a 9-anthryl group attached to an α-carbon, which is connected to a p-methylbenzyl group through an ether linkage. α-(9-anthryl)-p-methylbenzyl ethyl ether is known for its unique photophysical properties, making it a potential candidate for applications in fluorescence sensing and as a chromophore in materials science. Its structure allows for the investigation of intramolecular interactions and the study of electronic effects within the molecule. Due to its specific arrangement of aromatic rings and the presence of an ether group, it can be used in the development of new materials with tailored optical properties.

77033-11-5

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77033-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77033-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,3 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77033-11:
(7*7)+(6*7)+(5*0)+(4*3)+(3*3)+(2*1)+(1*1)=115
115 % 10 = 5
So 77033-11-5 is a valid CAS Registry Number.

77033-11-5Downstream Products

77033-11-5Relevant academic research and scientific papers

Reactions of (9-Anthryl)arylmethyl Chloride and Its Homologues with Nucleophiles under Solvolytic Conditions. Notable Effects of Reaction Conditions and Substituents on the Reaction Sites

Ogata, Fujimaro,Takagi, Masato,Nojima, Masatomo,Kusabayashi, Shigekazu

, p. 1145 - 1153 (2007/10/02)

The reactions of (9-anthryl)arylmethyl chlorides 2a-e (the substituents are p-MeO, p-Me, H, p-Cl, and m-Cl), the corresponding bromides 3b-d (the substituents are p-Me, H, and p-Cl), and the antimonate salts 4b-e (the substituents are p-Me, H, p-Cl, and m

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