1212-07-3

Basic information

• Product Name: N-(2-Pyridyl)benzenesulfonaMide, 97%
• Synonyms: N-(2-Pyridyl)benzenesulfonaMide, 97%
• CAS NO: 1212-07-3
• Molecular Formula: C₁₁H₁₀N₂O₂S
• Molecular Weight: 234.2743
• Mol File: 1212-07-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 407.8°Cat760mmHg
• Flash Point: 200.4°C
• Appearance: /
• Density: 1.363g/cm³
• Vapor Pressure: 7.36E-07mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: N-(2-Pyridyl)benzenesulfonaMide, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Pyridyl)benzenesulfonaMide, 97%(1212-07-3)
• EPA Substance Registry System: N-(2-Pyridyl)benzenesulfonaMide, 97%(1212-07-3)

Safety Data

• Hazardous Substances Data: 1212-07-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H10N2O2S/c14-16(15,10-6-2-1-3-7-10)13-11-8-4-5-9-12-11/h1-9H,(H,12,13)

Upstream product

• 15009-91-3 2-nitropyridine 
• 98-09-9 benzenesulfonyl chloride 
• 142-08-5 2-Pyridone 
• 72567-08-9 benzenesulfonylimine of hexafluoroacetone 
• 504-29-0 2-aminopyridine 
• 873-55-2 sodium benzenesulfonate 
• 109-04-6 2-bromo-pyridine 
• 98-10-2 benzenesulfonamide 

Relevant articles and documents

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.

Amidine Sulfonamides and Benzene Sulfonamides: Synthesis and Their Biological Evaluation

New amidine and benzene sulfonamide derivatives were developed and structures of the new products were confirmed by elemental and spectral analysis (FT-IR, ESI-MS, 1HNMR, and 13CNMR). In vitro, developed compounds were screened for t

Copper-catalyzed N-arylation of sulfonamides with aryl bromides under mild conditions

This Letter describes a copper catalyzed sulfonamide coupling reaction with aryl bromides to form N-aryl sulfonamides under mild conditions, including the first examples of Cu-catalyzed sulfonamide coupling at room temperature. The reaction protocol tolerates a broad range of substrates including a variety of primary and secondary sulfonamides and challenging heteroaryl bromides such as 2-bromothiazole.