64923-60-0

Basic information

• Product Name: 2-{[(methylsulfonyl)oxy]methyl}butyl methanesulfonate
• CAS NO: 64923-60-0
• Molecular Formula: C₇H₁₆O₆S₂
• Molecular Weight: 260.3283
• Mol File: 64923-60-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 465.8°C at 760 mmHg
• Flash Point: 235.5°C
• Density: 1.306g/cm³
• Vapor Pressure: 2.08E-08mmHg at 25°C
• Refractive Index: 1.469
• CAS DataBase Reference: 2-{[(methylsulfonyl)oxy]methyl}butyl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[(methylsulfonyl)oxy]methyl}butyl methanesulfonate(64923-60-0)
• EPA Substance Registry System: 2-{[(methylsulfonyl)oxy]methyl}butyl methanesulfonate(64923-60-0)

Safety Data

• Hazardous Substances Data: 64923-60-0(Hazardous Substances Data)

Usage

Chemical Class

Sulfonates

Composition

Butyl group (four carbon atoms), methanesulfonate group (linked through an oxygen atom), and methylsulfonyl group

Usage

Synthetic intermediate in organic chemistry

Applications

Production of pharmaceuticals, agrochemicals, and specialty chemicals

Solubility

High solubility in both organic and aqueous solutions

Industrial Use

Employed as a solvent in various industrial processes

Role

Reagent in the synthesis of organic molecules

Importance

Considered an important building block in the creation of complex chemical structures

Upstream product

• 2612-29-5 2-ethyl-1,3-propandiol 
• 124-63-0 methanesulfonyl chloride 
• 133-13-1 ethyl diethyl malonate 
• 26717-67-9 dimethyl ethylmalonate 

Relevant articles and documents

SULPHONAMIDES AND COMPOSITIONS THEREOF FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured: wherein the variables shown in Formula AA can be as defined anywhere herein. Compounds AA are modulators of NLRP1 and/or NLRP3

Pheromones and analogs from Neozeleboria wasps and the orchids that seduce them: a versatile synthesis of 2,5-dialkylated 1,3-cyclohexanediones

Chiloglottone, a wasp pheromone and attractant of sexually deceptive Chiloglottis orchids, and several structural analogs were synthesized. The synthetic approach is facile, high yielding and versatile, enabling rapid divergence to generate dialkylated analogs of chiloglottone. The key transformation was an organocadmium-mediated desymmetrization of glutaric anhydride derivatives. This library of synthetic 2,5-dialkylated 1,3-cyclohexanediones may assist in future identification of natural products in further species.