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N-methyl-N-(2-methoxyphenyl)-4-methylbenzenesulfonamide, also known as 4-Methyl-N-(2-methoxyphenyl)-N-methylbenzenesulfonamide, is a chemical compound with the molecular formula C15H17NO3S. It is a derivative of benzenesulfonamide, featuring a 4-methylbenzenesulfonamide core with an N-methyl group and a 2-methoxyphenyl group attached to the nitrogen atoms. N-methyl-N-(2-methoxyphenyl)-4-methylbenzenesulfonamide is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure. It is characterized by its ability to form hydrogen bonds and its potential to act as a chiral auxiliary in asymmetric synthesis. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the methoxy and methyl groups, making it a valuable building block in the development of new chemical entities.

6380-12-7

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6380-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6380-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6380-12:
(6*6)+(5*3)+(4*8)+(3*0)+(2*1)+(1*2)=87
87 % 10 = 7
So 6380-12-7 is a valid CAS Registry Number.

6380-12-7Relevant academic research and scientific papers

Copper-catalyzed intermolecular C-H amination of (Hetero)arenes via transient unsymmetrical λ3-iodanes

Sokolovs, Igors,Lubriks, Dmitrijs,Suna, Edgars

supporting information, p. 6920 - 6928 (2014/06/09)

A one-pot two-step method for intermolecular C-H amination of electron-rich heteroarenes and arenes has been developed. The approach is based on a room-temperature copper-catalyzed regioselective reaction of the in situ formed unsymmetrical (hetero)aryl-λ3-iodanes with a wide range of primary and secondary aliphatic amines and anilines.

Synthesis, structural characterization and biological screening of various sulfa drugs derived from 2-anisidine

Abbasi, Muhammad Athar,Aziz-Ur-Rehman,Muhmood, Tahir,Khan, Khalid Mohammed,Ashraf, Muhammad,Ejaz, Syeda Abida,Arshad, Samreen

, p. 404 - 410 (2013/07/27)

In the present study, a series of N-alkyl substituted sulfa drugs (sulfonamides) has been synthesized. The reaction of 2-anisidine (1) with 4-methylbenzenesulfonyl chloride (2) yielded N- (2-methoxyphenyl)-4- methylbenzenesulfonamide (3), which on bromina

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