103860-56-6

Basic information

• Product Name: 3-Pyridinesulfonanilide(6CI)
• Synonyms: 3-Pyridinesulfonanilide(6CI)
• CAS NO: 103860-56-6
• Molecular Formula: C₁₁H₁₀N₂O₂S
• Molecular Weight: 234.2743
• Product Categories: SULFONAMIDE
• Mol File: 103860-56-6.mol
• Article Data: 8

Chemical Properties

• Melting Point: 145 °C
• Boiling Point: 407.8±37.0 °C(Predicted)
• Appearance: /
• Density: 1.363±0.06 g/cm3(Predicted)
• PKA: 6.87±0.48(Predicted)
• CAS DataBase Reference: 3-Pyridinesulfonanilide(6CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinesulfonanilide(6CI)(103860-56-6)
• EPA Substance Registry System: 3-Pyridinesulfonanilide(6CI)(103860-56-6)

Safety Data

• Hazardous Substances Data: 103860-56-6(Hazardous Substances Data)

Upstream product

• 1692-25-7 3-pyridylboronic acid 
• 98-95-3 nitrobenzene 
• 16133-25-8 Pyridine-3-sulfonyl chloride 
• 62-53-3 aniline 
• 42899-76-3 pyridine-3-sulfonyl chloride hydrochloride 

Relevant articles and documents

Copper-Catalyzed Aminoarylation of Alkenes via Aminyl Radical Addition and Aryl Migration

We describe a new strategy for aminoarylation of alkenes by copper-catalyzed smiles rearrangement using O-benzoylhydroxylamines as the amine reagent. This method affords various β-amino amide derivatives possessing a quaternary carbon center with wide functional group tolerance and high regioselectivity. The mechanistic studies indicate that the transformation can involve aminyl radical intermediates under acid-free condition.

Synthesis of N-phenylsulfonamide derivatives and investigation of some esterase enzymes inhibiting properties

In this study, synthesis of nine N-phenylsulfonamide derivatives was designed by starting from aniline, which is the simplest aromatic amine. These compounds were obtained in yields between 69 and 95%. Inhibitory properties of synthesized compounds on car

Method for ultrasound-assisted synthesis of N-arylsulfonamide

The invention discloses a method for ultrasound-assisted synthesis of N-arylsulfonamide. N-arylsulfonamide compound is synthesized by series reaction of nitro reduction/sulfonyl chloride reduction/sulfonamidation with taking aromatic nitro compounds, sulfonyl chloride and iron powder as raw materials under ultrasonic stirring conditions. Water is used as a reaction medium and a hydrogen source inthe reaction. The method has the advantages of cheap and easily obtained raw materials, simple and mild reaction conditions, environmental friendliness, saving energy, high reaction selectivity and high yield, excellent compatibility of substrate functional groups and high application value.