24590-50-9

Basic information

• Product Name: 3-hydroxypropyl methanesulfonate
• CAS NO: 24590-50-9
• Molecular Formula: C₄H₁₀O₄S
• Molecular Weight: 154.1848
• Mol File: 24590-50-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 341.2°C at 760 mmHg
• Flash Point: 160.2°C
• Density: 1.29g/cm³
• Vapor Pressure: 5.37E-06mmHg at 25°C
• Refractive Index: 1.458
• CAS DataBase Reference: 3-hydroxypropyl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxypropyl methanesulfonate(24590-50-9)
• EPA Substance Registry System: 3-hydroxypropyl methanesulfonate(24590-50-9)

Safety Data

• Hazardous Substances Data: 24590-50-9(Hazardous Substances Data)

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 504-63-2 trimethyleneglycol 

Downstream Products

• 72320-38-8 3-azidopropan-1-ol 
• 805255-21-4 (1R,2S,3S,5S)-3-(4-Bromo-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]octane-2-carboxylic acid 3-methanesulfonyloxy-propyl ester 
• 398497-75-1 (1R,2S,3S,5S)-3-(4-Iodo-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]octane-2-carboxylic acid 3-methanesulfonyloxy-propyl ester 
• 398497-73-9 (1R,2S,3S,5S)-8-Methyl-3-p-tolyl-8-aza-bicyclo[3.2.1]octane-2-carboxylic acid 3-methanesulfonyloxy-propyl ester 

Relevant articles and documents

Mivacurium chloride intermediate and method for synthesizing Mivacurium Chloride using mivacurium chloride intermediate

The invention belongs to the technical field of synthesis of pharmaceutical compounds, and particularly discloses an improved Mivacurium Chloride intermediate suitable for industrial production and amethod for synthesizing Mivacurium Chloride using the mi

Selective catalytic sp3 C-O bond cleavage with C-N bond formation in 3-alkoxy-1-propanols

The ruthenium catalyzed selective sp3 C-O cleavage with amide formation was reported in reactions of 3-alkoxy-1-propanol derivatives and amines. The cleavage only occurs at the C3-O position even with 3-benzyloxy-1-propanol. Based on the experimental results, O-bound and C-bound Ru enolate complexes were proposed as key intermediates for the unique selective sp3 C-O bond cleavage in 3-alkoxy-1-propanols.

Aldoxime-substituted imidazolium derivatives useful in the treatment of poisoning by phosphorus-containing chemicals

A therapeutically effective class of low toxicity aldoxime-substituted functionalized imidazolium compounds and compositions is disclosed which is effective in the treatment of living species poisoned by organophosphorus chemicals which inactivate the enzyme acetylcholinesterase. In vivo administration of therapeutically effective amounts of these aldoxime-substituted imidazolium derivatives has been found to save mammals having inhibited acetylcholinesterase due to injection with lethal dosages of Soman.