59907-37-8

Basic information

• Product Name: Benzenesulfonamide, 4-methoxy-N,N-dimethyl-
• CAS NO: 59907-37-8
• Molecular Formula: C9H13NO3S
• Molecular Weight: 215.273
• Mol File: 59907-37-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methoxy-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methoxy-N,N-dimethyl-(59907-37-8)
• EPA Substance Registry System: Benzenesulfonamide, 4-methoxy-N,N-dimethyl-(59907-37-8)

Safety Data

• Hazardous Substances Data: 59907-37-8(Hazardous Substances Data)

Upstream product

• 103-83-3 N,N'-dimethylbenzylamine 
• 98-68-0 4-methoxy-phenyl-sulphonyl chloride 
• 87-52-5 3-(Dimethylaminomethyl)indole 
• 6140-09-6 sodium 4-methoxy-benzenesulfonate 
• 696-63-9 4-Methoxybenzenethiol 
• 68-12-2 N,N-dimethyl-formamide 
• 7010-86-8 N-methyl-4-methoxybenzenesulfonamide 
• 1774-47-6 trimethylsulfoxonium iodide 
• 100-66-3 methoxybenzene 
• 13360-57-1 dimethylamino sulfonyl chloride 
• 77-78-1 dimethyl sulfate 
• 124-40-3 dimethyl amine 
• 65651-95-8 3,3-Dimethyl-1-(4-methoxybenzolsulfonyl)-triazen 
• 186581-53-3 diazomethane 

Downstream Products

• 15020-57-2 N,N-dimethyl-4-hydroxybenzenesulfonamide 

Relevant articles and documents

Synthesis method of aryl tertiary sulfonamide compounds promoted by visible light

The invention provides a synthesis method of aryl tertiary sulfonamide compounds promoted by visible light. In a non-protonic solvent, N-benzyl tertiary amine and arylsulfonyl chloride are used as rawmaterials, under the conditions of photosensitizer catalysis and illumination, a reaction is carried out for 1-4h at room temperature, and then separation and purification are carried out to obtain the product. The synthesis method of the aryl tertiary sulfonamide compound provided by the invention has the advantages of mild reaction conditions, simplicity and convenience in operation, short reaction time, no need of any transition metal catalysis and environmental friendliness.

Preparation method of N,N-dimethylsulfamide derivatives

The invention discloses a preparation method of N,N-dimethylsulfamide derivatives and belongs to the technical field of synthesis of medical compounds. The preparation method comprises the following steps: reacting gramine, a reactant with sulfonyl chloride groups and an alkaline substance with any one of solvents such as CH2Cl2, CH3COCH3 and CH3CN at a temperature of minus 15 DEG C to 80 DEG C for 24-48 hours so as to obtain the product, wherein the molar ratio of the gramine to the reactant to the alkaline substance is (1.0-2.0):(1.2-4.0):(1.5-6.0). The N,N-dimethylsulfamide derivatives can be simply and efficiently prepared withlow cost, and the yield is up to 70-98%.

Potassium tert-butoxide-mediated metal-free synthesis of sulfonamides from sodium sulfinates and N,N-disubstituted formamides

By using formamides as amine sources, a novel and efficient KO-t-Bu mediated amination of sodium sulfinates has been developed. The reaction utilizes readily available starting materials under metal-free conditions, thus providing an alternative and attractive route to sulfonamides.