141666-92-4

Basic information

• Product Name: Benzenesulfonamide, N-[2-(4-methoxyphenyl)ethyl]-4-methyl-
• CAS NO: 141666-92-4
• Molecular Formula: C16H19NO3S
• Molecular Weight: 305.398
• Mol File: 141666-92-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-[2-(4-methoxyphenyl)ethyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-[2-(4-methoxyphenyl)ethyl]-4-methyl-(141666-92-4)
• EPA Substance Registry System: Benzenesulfonamide, N-[2-(4-methoxyphenyl)ethyl]-4-methyl-(141666-92-4)

Safety Data

• Hazardous Substances Data: 141666-92-4(Hazardous Substances Data)

Upstream product

• 1258181-24-6 C₁₉H₂₀Cl₃NO₅S 
• 159690-31-0 1-p-Toluolsulfonyl-1-phenethyl-hydrazin 
• 151259-26-6 C₁₉H₃₄N₂O₂S 
• 146404-40-2 1-tosyl-1-hexadecylhydrazine 
• 146404-41-3 C₁₅H₁₇ClN₂O₂S 
• 141666-91-3 N-[2-(4-chlorophenyl)ethyl]-4-methylbenzenesulfonamide 
• 18049-99-5 N-hexadecyl-p-toluenesulfonamide 
• 1635-09-2 N-dodecyl-4-methylbenzenesulfonamide 
• 5450-75-9 4-methyl-N-(2-phenylethyl)benzenesulfonamide 
• 536-57-2 p-toluene sulfinic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 55-81-2 4-Methoxyphenethylamine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 14425-64-0 4-methoxyphenethyl bromide 
• 5450-75-9 4-methyl-N-(2-phenylethyl)benzenesulfonamide 
• 1635-09-2 N-dodecyl-4-methylbenzenesulfonamide 
• 18049-99-5 N-hexadecyl-p-toluenesulfonamide 
• 1950-69-2 toluene-p-sulfonyl bromide 
• 141666-91-3 N-[2-(4-chlorophenyl)ethyl]-4-methylbenzenesulfonamide 
• 146404-41-3 C₁₅H₁₇ClN₂O₂S 
• 146404-40-2 1-tosyl-1-hexadecylhydrazine 
• 98-59-9 p-toluenesulfonyl chloride 
• 151259-26-6 C₁₉H₃₄N₂O₂S 
• 159690-31-0 1-p-Toluolsulfonyl-1-phenethyl-hydrazin 

Relevant articles and documents

Cyclometalated Ru(II)-isoquinoline complexes overcome cisplatin resistance of A549/DDP cells by downregulation of Nrf2 via Akt/GSK-3β/Fyn pathway

Both ruthenium (Ru) and isoquinoline (IQ) compounds are regarded as potential anticancer drug candidates. Here, we report the synthesis and characterization of three novel cyclometalated Ru(II)-isoquinoline complexes: RuIQ-3, RuIQ-4, and RuIQ-5, and evalu

Synthesis, enzyme inhibitory kinetics mechanism and computational study of N-(4-methoxyphenethyl)-N-(substituted)- 4-methylbenzenesulfonamides as novel therapeutic agents for Alzheimer's disease

The present study comprises the synthesis of a new series of sulfonamides derived from 4-methoxyphenethylamine (1). The synthesis was initiated by the reaction of 1 with 4-methylbenzenesulfonyl chloride (2) in aqueous sodium carbonate solution at pH 9 to

SUBSTITUTED ALKYL DIARYL DERIVATIVES, METHODS OF PREPARATION AND USES

Compounds according to Formula I are provided: and salts thereof, wherein Q1, Q2, R3, R4, X, and Y are as defined herein. Methods for preparing compounds of Formula I are also provided, as well as methods of tre