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4-(m-tolyloxy)pyridine is an organic compound characterized by its molecular formula C12H11NO, which consists of a pyridine ring with a methoxy group attached to the meta position of a tolyl group. 4-(m-tolyloxy)pyridine is a derivative of pyridine, a heterocyclic aromatic compound with a nitrogen atom in the ring. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure. The compound's properties, such as its reactivity and solubility, can be influenced by the presence of the methoxy group, which can participate in hydrogen bonding and affect the molecule's electronic properties. 4-(m-tolyloxy)pyridine is typically synthesized through chemical reactions involving pyridine and its derivatives, and it is an important intermediate in the preparation of more complex molecules.

4979-02-6

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4979-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4979-02-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4979-02:
(6*4)+(5*9)+(4*7)+(3*9)+(2*0)+(1*2)=126
126 % 10 = 6
So 4979-02-6 is a valid CAS Registry Number.

4979-02-6Downstream Products

4979-02-6Relevant academic research and scientific papers

Low catalyst loadings for copper-catalyzed O-arylation of phenols with aryl and heteroaryl halides under mild conditions

Yong, Fui-Fong,Teo, Yong-Chua,Yan, Yaw-Kai,Chua, Guan-Leong

supporting information; experimental part, p. 101 - 106 (2012/02/03)

A practical and mild strategy has been developed for the cross-coupling of O-arylation of phenol with differently substituted aryl halides and heteroaryl iodides using low catalyst loading of copper iodide under low operating temperature in DMF with TMHD as the ligand and Cs2CO3 as the base. This method tolerates a variety of functional groups including sterically hindered phenols and heteroaryl iodides to afford products in good to excellent yields (up to 95%). Georg Thieme Verlag Stuttgart. New York.

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