1352947-63-7

Basic information

• Product Name: 1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate
• Synonyms: 1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate;1-Methyl-3-[6-(methylthio)hexyl]imidazolium p-Toluenesulfonate
• CAS NO: 1352947-63-7
• Molecular Formula: C₇H₇O₃S*C₁₁H₂₁N₂S
• Molecular Weight: 384.55652
• Mol File: 1352947-63-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Water Solubility: Slightly soluble in water
• CAS DataBase Reference: 1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate(1352947-63-7)
• EPA Substance Registry System: 1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate(1352947-63-7)

Safety Data

• Hazardous Substances Data: 1352947-63-7(Hazardous Substances Data)

Usage

General Description

1-Methyl-3-[6-(Methylthio)hexyl]iMidazoliuM p-Toluenesulfonate is a chemical compound that acts as a sedative and anesthetic. It is a derivative of the imidazole family and is used in the pharmaceutical industry for its sedative-hypnotic properties. The compound has a p-toluenesulfonate salt form, which allows for increased stability and solubility in a variety of solvents. It is commonly administered intravenously for sedation and anesthesia in medical procedures. The presence of the methylthio and hexyl groups in the compound's structure contributes to its pharmacological activity and makes it an important component in the field of anesthesia.

Upstream product

• 1633-78-9 6-mercapto-1-hexanol 
• 98433-41-1 6-(methylthio)hexan-1-ol 
• 2009-83-8 6-chloro-1-hexanol 
• 616-47-7 1-methyl-1H-imidazole 
• 139450-84-3 6-(methylthio)hexyl 4'-methylbenzenesulfonate 

Relevant articles and documents

Efficient Swern oxidation and Corey-Kim oxidation with ion-supported methyl sulfoxides and methyl sulfides

The Swern oxidation of various benzylic and allylic alcohols, primary alcohols, and secondary alcohols with two ion-supported methyl sulfoxides A-1 (C6) and B-1 (C10), and oxalyl chloride in the presence of triethylamine in dichloromethane, followed by simple diethyl ether extraction of the reaction mixture, gave the corresponding aldehydes and ketones, respectively, in good yields with high purity. Similarly, the Corey-Kim oxidation of various benzylic and allylic alcohols, primary alcohols, and secondary alcohols with two ion-supported methyl sulfides A-2 (C6) and B-2 (C10), and N-chlorosuccinimide in the presence of triethylamine in dichloromethane, followed by simple diethyl ether extraction of the reaction mixture, furnished the corresponding aldehydes and ketones, respectively, in good yields with high purity. Both reactions did not produce any unpleasant odor at all. In the Swern oxidation, ion-supported methyl sulfides were recovered in high yields and could be re-oxidized to produce ion-supported methyl sulfoxides A-1 (C6) and B-1 (C10), for reuse in the same oxidation. In the Corey-Kim oxidation, ion-supported methyl sulfides A-2 (C6) and B-2 (C10) were recovered in high yields and could be also reused for the same oxidation.