39996-41-3

Basic information

• Product Name: 1-aminopyridinium mesitylenesulphonate
• Synonyms: 1-aminopyridinium mesitylenesulphonate
• CAS NO: 39996-41-3
• Molecular Weight: 294.375
• Mol File: 39996-41-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-aminopyridinium mesitylenesulphonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-aminopyridinium mesitylenesulphonate(39996-41-3)
• EPA Substance Registry System: 1-aminopyridinium mesitylenesulphonate(39996-41-3)

Safety Data

• Hazardous Substances Data: 39996-41-3(Hazardous Substances Data)

Usage

Chemical composition

1-aminopyridinium cation and mesitylenesulphonate anion.

Physical state

Crystalline material.

Category

Organic salt.

Usage

Chemical intermediate in organic synthesis.

Application

Building block for constructing functional materials.

Potential use

Organic light-emitting diodes and optoelectronic devices.

Field of interest

Materials science and organic chemistry.

Upstream product

• 110-86-1 pyridine 
• 36016-40-7 mesitylenesulfonylhydroxylamine 

Downstream Products

• 17408-39-8 3-benzoyl-2-phenylpyrazolo<1,5-a>pyridine 
• 81460-43-7 C₁₆H₁₈N₂O 
• 40949-56-2 N-(p-toluenesulphonylimino)pyridinium ylide 
• 1005774-67-3 2-benzyl-4-(2-isopropylpyrazolo[1,5-a]pyridin-3-yl)phthalazin-1(2H)-one 
• 1005774-62-8 6-(2-isopropylpyrazolo[1,5-a]pyridin-3-yl)-2-phenylpyridazin-3(2H)-one 
• 1005774-56-0 2-benzyl-6-(2-isopropylpyrazolo[1,5-a]pyridin-3-yl)pyridazin-3(2H)-one 
• 122643-81-6 2-phenyl-3-acetylpyrazolo[1,5-a]pyridine 
• 87290-00-4 1-pyridinio(p-toluenethiocarbonyl)amidate 
• 106-49-0 p-toluidine 
• 108-44-1 1-amino-3-methylbenzene 
• 95-53-4 o-toluidine 
• 19364-00-2 1-Benzoylpyrazolo<1,5-a>pyridine 
• 63237-84-3 methyl pyrazolo<1,5-a>pyridine-3-carboxylate 
• 59942-95-9 1-Acetylpyrazolo<1,5-a>pyridine 

Relevant articles and documents

Heteroaryl imidazolone derivatives as jak inhibitors

New heteroaryl imidazolone derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).

Structure-kinetics relations holding in the amination of six-membered nitrogen-containing heterocyclic compounds

Relative rates of the amination of 3-X- and 4-X-substituted pyridines (X = H, 3-Me, 4-Me, 3-F3C, 3-CN, 4-CN, 3-Cl, 3-Br, 4-MeO, 4-Me 2N), pyrazine, quinoline, isoquinoline, 2,2′- and 4,4′-bipyridines, and 1,10-phenanthroline with O-

Synthesis of N-benzoylamino-1,2,3,6-tetrahydropyridine derivatives as potential anti-inflammatory agents

(Chemical Equation Presented) N-Benzoylamino-1,2,3,6-tetrahydropyridines 9a-q were synthesized from 4-substituted pyridines in four steps. Amination of pyridines was carried out to prepare intermediate N-aminopyridinium mesylates using mesytelenesulfonyl hydroxmate (MSH) as aminating agent. N-aminopyridinium mestylates reacted with appropriately substituted acyl chlorides to form N-ylides as stable crystalline solids. Partial reduction of N-ylides with mild reducing agent afforded N-benzoylamino-1,2,3,6-tetrahydropyridines in fair to good yields.