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(4-chloro-phenyl)-(3-fluoro-benzyl)-ether is an organic compound characterized by its molecular structure, which features a benzyl group connected to a chlorophenyl group through an ether linkage. The chlorophenyl group contains a chlorine atom at the 4th position, while the benzyl group has a fluorine atom at the 3rd position. (4-chloro-phenyl)-(3-fluoro-benzyl)-ether is a member of the aryl ether class, which are known for their potential applications in various chemical and pharmaceutical processes. Due to the presence of halogenated substituents, it may exhibit unique reactivity and properties compared to non-halogenated aryl ethers. The specific combination of chlorine and fluorine atoms can influence its electronic properties, making it a compound of interest for researchers in the field of organic chemistry.

332-02-5

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332-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332-02-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 332-02:
(5*3)+(4*3)+(3*2)+(2*0)+(1*2)=35
35 % 10 = 5
So 332-02-5 is a valid CAS Registry Number.

332-02-5Downstream Products

332-02-5Relevant academic research and scientific papers

Synthesis and anti-cancer activities of aryl benzyl ethers with fluoro substituents

Jiang, Yi,Xu, Hong,Liu, Li,He, Rui,Song, Xiaomei,Li, Na

, p. 736 - 741 (2014/07/07)

A series of aryl benzyl ethers with fluoro substituents were synthesized and their structures were confirmed by spectral. All the compounds were tested for their cytotoxic activity in vitro against two human tumor cell lines: A549, SGC7901, and most showed cytotoxicity. Compound 10 was the most active in suppressing the growth of both screened cancer cells.

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