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α-Anisyl-9-anthrylmethylethylether is a complex organic compound characterized by its unique molecular structure, which consists of an anthracene moiety, an anisyl group, and an ethyl ether linkage. α-Anisyl-9-anthrylmethylethylether is known for its distinct fluorescence properties, making it a potential candidate for applications in the field of chemosensing and as a fluorophore in various analytical techniques. The anthracene unit provides a strong fluorescence signal, while the anisyl group offers a degree of solubility and stability in different solvents. The ethyl ether linkage further contributes to the compound's solubility and can influence its reactivity. α-Anisyl-9-anthrylmethylethylether is synthesized through a series of chemical reactions and is typically used in research settings to study molecular interactions and develop new materials with specific optical properties.

71032-59-2

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71032-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71032-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,3 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71032-59:
(7*7)+(6*1)+(5*0)+(4*3)+(3*2)+(2*5)+(1*9)=92
92 % 10 = 2
So 71032-59-2 is a valid CAS Registry Number.

71032-59-2Downstream Products

71032-59-2Relevant 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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