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(4-fluoro-phenyl)-(4-methyl-benzyl)-ether is an organic compound characterized by its molecular formula C15H13FO. It is a derivative of phenyl ether, with a fluorine atom substituting one hydrogen atom on the phenyl ring and a 4-methyl-benzyl group attached to the oxygen atom. (4-fluoro-phenyl)-(4-methyl-benzyl)-ether is known for its aromatic structure and potential applications in the synthesis of pharmaceuticals and other organic compounds. It is a colorless liquid with a distinct aromatic odor and is insoluble in water but soluble in organic solvents. Due to its specific functional groups, it can participate in various chemical reactions, such as nucleophilic aromatic substitution and electrophilic aromatic substitution, making it a versatile building block in organic chemistry.

351-68-8

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351-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351-68-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 351-68:
(5*3)+(4*5)+(3*1)+(2*6)+(1*8)=58
58 % 10 = 8
So 351-68-8 is a valid CAS Registry Number.

351-68-8Downstream Products

351-68-8Relevant academic research and scientific papers

Pd(OAc)2-catalyzed synthesis of benzyl phenyl ether derivatives with H2O2 as an oxidant in neat water

Chen, Qian-Qian,Zhang, Hui-Xian,Yang, Jian-Xin

, p. 115 - 118 (2018/11/10)

A new protocol for Pd(OAc)2-catalyzed reactions of different benzyl bromides and various arylboronic acids has been developed to form functionalized benzyl phenyl ethers. This method represents the first instance where arylboronic acid is used as a reaction substrate for benzyl phenyl ether synthesis with H2O2 as the green oxidant under atmospheric oxygen and pure H2O as an environmental friendly solvent without the requirement for phosphine- and N-based ligands, remarkable functional group tolerance, and considerable yield.

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