85838-93-3

Basic information

• Product Name: 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine
• Synonyms: 1-(Phenylsulfonyl)-1,2,3,6-tetrahydropyridine; pyridine, 1,2,3,6-tetrahydro-1-(phenylsulfonyl)-
• CAS NO: 85838-93-3
• Molecular Formula: C₁₁H₁₃NO₂S
• Molecular Weight: 223.2914
• Mol File: 85838-93-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 357.9°C at 760 mmHg
• Flash Point: 170.2°C
• Density: 1.253g/cm³
• Vapor Pressure: 2.65E-05mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine(85838-93-3)
• EPA Substance Registry System: 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine(85838-93-3)

Safety Data

• Hazardous Substances Data: 85838-93-3(Hazardous Substances Data)

Usage

General Description

1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine is a chemical compound with the molecular formula C11H13NO2S. It is a derivative of tetrahydropyridine that contains a phenylsulfonyl group attached to the nitrogen atom of the ring. 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine has potential applications in medicinal chemistry, particularly in the development of drugs targeting neurological disorders. The presence of the sulfonyl group may confer certain pharmacological properties, and its molecular structure makes it a valuable building block in the synthesis of more complex molecules. Research into the biological and chemical properties of 1-(phenylsulfonyl)-1,2,3,6-tetrahydropyridine is ongoing, and it may hold promise for future therapeutic developments.

Downstream Products

• 85838-97-7 ((3S,4R)-1-Benzenesulfonyl-3-hydroxy-piperidin-4-yl)-carbamic acid tert-butyl ester 
• 85838-98-8 ((3S,4R)-1-Benzenesulfonyl-4-hydroxy-piperidin-3-yl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Cycloalkyl-based unsymmetrical unsaturated (U2)-NHC ligands: Flexibility and dissymmetry in ruthenium-catalysed olefin metathesis

Air-stable Ru-indenylidene and Hoveyda-type complexes bearing new unsymmetrical unsaturated N-heterocyclic carbene (U2-NHC) ligands combining a mesityl unit and a flexible cycloalkyl moiety as N-substituents were synthesised. Structural features, chemical stabilities and catalytic profiles in olefin metathesis of this new library of cycloalkyl-based U2-NHC Ru complexes were studied and compared with their unsymmetrical saturated NHC-Ru homologues as well as a set of commercially available Ru-catalysts bearing either symmetrical SIMes or IMes NHC ligands.