1352947-66-0

Basic information

• Product Name: 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate
• Synonyms: 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate;1-Methyl-3-[6-(methylsulfinyl)hexyl]imidazolium p-Toluenesulfonate
• CAS NO: 1352947-66-0
• Molecular Formula: C₇H₇O₃S*C₁₁H₂₁N₂OS
• Molecular Weight: 400.55592
• Mol File: 1352947-66-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Solubility: slightly sol. in Methanol
• CAS DataBase Reference: 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate(1352947-66-0)
• EPA Substance Registry System: 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate(1352947-66-0)

Safety Data

• Hazardous Substances Data: 1352947-66-0(Hazardous Substances Data)

Usage

General Description

1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate, also known by its chemical formula C20H27N3O4S, is a pharmaceutical compound used as a sedative and anxiolytic. It is a salt form of the drug midazolam, which is commonly administered for sedation and anesthesia in medical procedures. This specific form of midazolam is p-toluenesulfonate, which is a crystalline powder that is soluble in water and alcohol. It is used primarily in hospitals and clinical settings under the supervision of a healthcare professional. As a sedative, it acts on the central nervous system to induce relaxation, drowsiness, and relieve anxiety. 1-Methyl-3-[6-(Methylsulfinyl)hexyl]iMidazoliuM p-Toluenesulfonate should only be used under the guidance of a qualified medical professional due to its potential for side effects and interactions with other medications.

Upstream product

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

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.