86328-85-0

Basic information

• Product Name: N-(cyclohexylmethyl)-4-methylbenzenesulfonamide
• Synonyms: N-(cyclohexylmethyl)-4-methylbenzenesulfonamide
• CAS NO: 86328-85-0
• Molecular Weight: 267.392
• Mol File: 86328-85-0.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: N-(cyclohexylmethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(cyclohexylmethyl)-4-methylbenzenesulfonamide(86328-85-0)
• EPA Substance Registry System: N-(cyclohexylmethyl)-4-methylbenzenesulfonamide(86328-85-0)

Safety Data

• Hazardous Substances Data: 86328-85-0(Hazardous Substances Data)

Upstream product

• 593-71-5 Chloroiodomethane 
• 260975-29-9 (E)-N-cyclohexylmethylene-4-toluenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 100-49-2 cyclohexylmethyl alcohol 
• 88-19-7 methyl 2-(aminosulfonyl)benzoate 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 2043-61-0 cyclohexanecarbaldehyde 
• 110-82-7 cyclohexane 
• 640-61-9 N-methyl-p-toluenesulfonylamide 
• 175355-34-7 N-(cyclohexylmethylene)-4-methylbenzenesulfonamide 
• 13698-06-1 N-(cyclohexa-1,4-dienylmethyl)-4-methylbenzenesulfonamide 

Downstream Products

• 3218-02-8 cyclohexylmethylamine 
• 260975-29-9 (E)-N-cyclohexylmethylene-4-toluenesulfonamide 

Relevant articles and documents

Diiodine-Triethylsilane System: Reduction of N-Sulfonyl Aldimines to N-Alkylsulfonamides

Because molecular iodine and hydrosilanes are stable to both air and moisture, reactions using these reagents are easy to operate and require mild reaction conditions. Molecular iodine and a hydrosilane were used to reduce N-sulfonyl aldimines to the corr

Ni(0)-Catalyzed Three-Component Coupling Reaction of Tetrafluoroethylene and N-Sulfonyl-Substituted Imines with Silanes via Aza-Nickelacycles

A nickel-catalyzed three-component coupling reaction of tetrafluoroethylene (TFE) and N-sulfonyl-substituted imines with silanes that furnishes a variety of fluorine-containing amines is disclosed. Stoichiometric experiments revealed that the aza-nickelac

A synthetic N-alkyl sulfonamide derivatives

The invention discloses a method for synthesizing a N-alkyl sulfonamide derivative. The method comprises the following steps: adding a sulfonamide derivative, a water-soluble catalyst, an alkali, alcohol and a solvent into a reaction container; reacting the reaction mixture at 100-120 DEG C for several hours, cooling to room temperature; performing rotary evaporation to remove the solvent, and then separating by a column to obtain the target compound. The method of the invention starts from the sulfonamide derivative, and obtains the N-alkyl sulfonamide derivative through reaction with alcohol. The method of the invention adopts a water-soluble iridium complex as a catalyst; the reaction is carried out in water; and the target compound is obtained with a high yield. Therefore, the reaction meets the requirements for green chemistry, and the method has wide development prospects.