17075-14-8

Basic information

• Product Name: 2-(methylsulfonyl)pyridine
• Synonyms: 2-(methylsulfonyl)pyridine
• CAS NO: 17075-14-8
• Molecular Formula: C₆H₇NO₂S
• Molecular Weight: 157.19
• Mol File: 17075-14-8.mol
• Article Data: 34

Chemical Properties

• Boiling Point: 340.9 °C at 760 mmHg
• Flash Point: 160 °C
• Appearance: /
• Density: 1.263 g/cm³
• Vapor Pressure: 0.000165mmHg at 25°C
• Refractive Index: 1.522
• PKA: -1.59±0.12(Predicted)
• CAS DataBase Reference: 2-(methylsulfonyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(methylsulfonyl)pyridine(17075-14-8)
• EPA Substance Registry System: 2-(methylsulfonyl)pyridine(17075-14-8)

Safety Data

• Hazardous Substances Data: 17075-14-8(Hazardous Substances Data)

Usage

General Description

2-(methylsulfonyl)pyridine is a chemical compound with the molecular formula C6H7NO2S. It is a member of the pyridine family and contains a methylsulfonyl group attached to the pyridine ring. The compound is used in the synthesis of pharmaceuticals and agrochemicals, and as a building block in organic chemistry. It is also a potential intermediate in the production of various functionalized pyridines. 2-(methylsulfonyl)pyridine has potential applications in the fields of medicine, agriculture, and material science, and its chemical and physical properties make it a versatile and valuable compound for research and development.

InChI:InChI=1/C6H7NO2S/c1-10(8,9)6-4-2-3-5-7-6/h2-5H,1H3

Upstream product

• 18438-38-5 2-methylsulfanyl-pyridine 
• 74-88-4 methyl iodide 
• 2637-34-5 2-Sulfanylpyridine 
• 21948-75-4 2-methylsulfinylpyridine 
• 10213-10-2 sodium tungstate (VI) dihydrate 
• 109-09-1 2-chloropyridine 
• 13737-04-7 2-(trimethylsilyl)pyridine 
• 109-04-6 2-bromo-pyridine 
• 20277-69-4 sodium methansulfinate 
• 124-63-0 methanesulfonyl chloride 
• 1219454-89-3 2-((difluoromethyl)sulfonyl)pyridine 
• 15796-89-1 N-methyl-N-phenylmethacrylamide 

Downstream Products

• 928768-94-9 (E)-2-((2-phenylprop-1-en-1-yl)sulfonyl)pyridine 

Relevant articles and documents

COMPOSITES, METHODS AND USES THEREOF

The present invention relates, in general terms, to methods of catalysing a reaction, including the steps of contacting a chemical entity comprising a sulphide moiety with a composite and an oxidant. The composite acts as a heterogeneous catalyst to oxidise the sulphide moiety. The present invention also relates to composites, methods of synthesising the composites and its use as a catalyst thereof.

Flow Electrosynthesis of Sulfoxides, Sulfones, and Sulfoximines without Supporting Electrolytes

An efficient electrochemical flow process for the selective oxidation of sulfides to sulfoxides and sulfones and of sulfoxides toN-cyanosulfoximines has been developed. In total, 69 examples of sulfoxides, sulfones, andN-cyanosulfoximines have been synthesized in good to excellent yields and with high current efficiencies. The synthesis was assisted and facilitated through a supporting electrolyte-free, fully automated electrochemical protocol that highlights the advantages of flow electrolysis.

Selective oxidation of (hetero)sulfides with molecular oxygen under clean conditions

The development of eco-friendly and switchable catalytic systems for the conversion of a sole raw-material into distinct high-value products is a particularly attractive concept and a daunting synthetic challenge. In the present work, the first example of efficient and selective oxidation of sulfides to sulfones and sulfoxides using molecular oxygen under clean conditions was established.