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N,4-dimethyl-N-(m-tolyl)benzenesulfonamide is a chemical compound with the molecular formula C15H17NO2S. It is an organic compound that belongs to the class of sulfonamides, which are derivatives of benzene with a sulfonamide group attached. This specific compound features a benzene ring with two methyl groups at the N and 4 positions, and a m-tolyl group (a methyl-substituted phenyl group) attached to the nitrogen atom. It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its chemical structure, it exhibits properties such as solubility in organic solvents and reactivity with nucleophiles. The compound's synthesis typically involves the reaction of a suitable benzenesulfonamide with an appropriate m-tolyl halide or other electrophilic reagents.

6927-50-0

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6927-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6927-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6927-50:
(6*6)+(5*9)+(4*2)+(3*7)+(2*5)+(1*0)=120
120 % 10 = 0
So 6927-50-0 is a valid CAS Registry Number.

6927-50-0Downstream Products

6927-50-0Relevant academic research and scientific papers

Charge-Transfer Complex Promoted Regiospecific C?N Bond Cleavage of Vicinal Tertiary Diamines

Fu, Ying,Xu, Qin-Shan,Shi, Chun-Zhao,Du, Zhengyin,Xiao, Caiqin

, p. 3502 - 3506 (2018)

A catalyst-free, charge-transfer complex promoted coupling of sulfonyl chlorides with vicinal tertiary diamines to generate sulfonamides is presented. Mechanistic studies showed that these reactions are proceeded via charge transfer of vicinal tertiary diamines to sulfonyl chlorides, forming the unstable sulfonyl quaternary ammonium like complexes which induced the regiospecific intramolecular C?N bond cleavage of vicinal tertiary diamines. (Figure presented.).

NaI-Catalyzed Oxidative Amination of Aromatic Sodium Sulfinates: Synergetic Effect of Ethylene Dibromide and Air as Oxidants

Fu, Ying,Li, Quan-Zhou,Xu, Qin-Shan,Hügel, Helmut,Li, Ming-Peng,Du, Zhengyin

supporting information, p. 6966 - 6970 (2018/11/23)

A novel NaI-catalyzed oxidative amination of sodium sulfinates, employing both ethylene dibromide (EDB) and air as the oxidants, is described. EDB was first demonstrated to be a promising mild organic oxidant that in air, converted NaI into molecular iodine to promote the cross-coupling reactions of aromatic sodium sulfinates with amines to produce arylsulfonamides. Mechanistic studies indicated that a radical pathway might be involved in the reaction process.

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