2058-49-3

Basic information

• Product Name: METHYL-(3-HYDROXYPROPYL) SULFONE
• Synonyms: 3-(methylsulfonyl)-1-propano;3-hydroxypropylmethylsulfone;METHYL-(3-HYDROXYPROPYL) SULFONE;3-(Methylsulfonyl)-1-propanol;3-(methylsulfonyl)-1-propanol(SALTDATA: FREE);3-(Methylsulfonyl)propan-1-ol;3-(Methanesulfonyl)-1-propanol;Ba 2769
• CAS NO: 2058-49-3
• Molecular Formula: C₄H₁₀O₃S
• Molecular Weight: 138.19
• Mol File: 2058-49-3.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 349.4°Cat760mmHg
• Flash Point: 165.1°C
• Appearance: /
• Density: 1.221g/cm³
• Vapor Pressure: 2.86E-06mmHg at 25°C
• Refractive Index: 1.458
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.57±0.10(Predicted)
• CAS DataBase Reference: METHYL-(3-HYDROXYPROPYL) SULFONE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL-(3-HYDROXYPROPYL) SULFONE(2058-49-3)
• EPA Substance Registry System: METHYL-(3-HYDROXYPROPYL) SULFONE(2058-49-3)

Safety Data

• Hazard Codes: T
• Statements: 25-36
• Safety Statements: 26-45
• RIDADR: UN 2811 6.1 / PGIII
• WGK Germany: 3
• HazardClass: IRRITANT
• PackingGroup: Ⅲ
• Hazardous Substances Data: 2058-49-3(Hazardous Substances Data)

Usage

General Description

Methyl-(3-Hydroxypropyl) Sulfone is an organic compound with the chemical formula C4H10O3S. It is commonly known as Methylsulfonylmethane (MSM) and is found in a variety of foods including fruits, vegetables, and grains. It is also used as a dietary supplement to promote joint health and reduce inflammation. Additionally, MSM is used in some skincare products for its potential to improve skin health and reduce signs of aging. Its potential benefits are attributed to its anti-inflammatory and antioxidant properties, although more research is needed to fully understand its effects on the body.

InChI:InChI=1/C4H10O3S/c1-8(6,7)4-2-3-5/h5H,2-4H2,1H3

Upstream product

• 17696-73-0 methylsulfinic acid 
• 627-18-9 1-bromo-3-propanol 
• 505-10-2 3-(methylthio)-1-propanol 
• 20277-69-4 sodium methansulfinate 
• 64741-01-1 m-chloroperoxybenzoic acid 
• 7757-83-7 sodium sulfite 

Downstream Products

• 357913-53-2 methanesulfonic acid 3-methanesulfonyl-propyl ester 
• 205193-46-0 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(3(methylsulphonyl)propoxy)quinazoline hydrochloride 
• 1429427-45-1 1-bromo-2-((3-(methylsulfonyl)propoxy)methyl)benzene 
• 1429427-46-2 1-bromo-3-((3-(methylsulfonyl)propoxy)methyl)benzene 
• 263400-88-0 3-(methylsulfonyl)propyl 4-methylbenzenesulfonate 
• 1426800-61-4 5-(4-cyano-phenyl)-2-(3-methanesulfonyl-propyl)-7-methyl-3-oxo-8-(3-trifluoromethyl-phenyl)-2,3,5,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrimidine-6-carboxylic acid methyl ester 
• 859940-73-1 1-bromo-3-(methylsulphonyl)propane 
• 883-44-3 N-(3-hydroxypropyl)phthalimide 

Relevant articles and documents

Selective synthesis of sulfoxides and sulfonesviacontrollable oxidation of sulfides withN-fluorobenzenesulfonimide

A practical and mild method for the switchable synthesis of sulfoxides or sulfonesviaselective oxidation of sulfides using cheapN-fluorobenzenesulfonimide (NFSI) as the oxidant has been developed. These highly chemoselective transformations were simply achieved by varying the NFSI loading with H2O as the green solvent and oxygen source without any additives. The good functional group tolerance makes the strategy valuable.

Imidazole derivative used as antiviral agent and use thereof in preparation of medicament

Disclosed are an antiviral compound and a use thereof in the preparation of a medicament for the treatment of virus infections. Specifically, the present invention relates an imidazole derivative for treating respiratory syncytial virus infection.

SPIRO UREA COMPOUNDS AS RSV ANTIVIRAL COMPOUNDS

The invention concerns novel substituted spiro urea azetidinyl or piperidinyl compounds of formula (I) having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention furth