3445-78-1

Basic information

• Product Name: Pyridino[5',6':2,3]trithione
• Synonyms: Pyridino[5',6':2,3]trithione;[1,2]dithiolo[5,4-b]pyridine-3-thione;1,2-Dithiolo[3,4-b]pyridine-3-thione;3-dithiolo[5,4-b]pyridinethione;dithiolo[5,4-b]pyridine-3-thione
• CAS NO: 3445-78-1
• Molecular Formula: C₆H₃NS₃
• Molecular Weight: 185.28972
• Mol File: 3445-78-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Pyridino[5',6':2,3]trithione(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridino[5',6':2,3]trithione(3445-78-1)
• EPA Substance Registry System: Pyridino[5',6':2,3]trithione(3445-78-1)

Safety Data

• Hazardous Substances Data: 3445-78-1(Hazardous Substances Data)

Usage

General Description

Pyridino[5',6':2,3]trithione is a chemical compound with the molecular formula C6H5N3S3. It is a tricyclic heterocyclic compound containing a pyridine ring fused to a trithione ring. Pyridino[5',6':2,3]trithione is primarily used in the synthesis of organic compounds and materials. It has also been studied for its potential use in pharmaceuticals and agrochemicals due to its unique structural properties. Pyridino[5',6':2,3]trithione is known for its interesting and diverse reactivity, making it a valuable intermediate in organic synthesis and a subject of research in various scientific fields.

Upstream product

• 65282-42-0 1,2-dithiolo<5,4-b>pyridin-3-one 
• 65282-47-5 2-butylisothiazolo<5,4-b>pyridin-3(2H)-one 
• 330667-58-8 2-mercapto-N-phenethyl-nicotinamide 
• 330667-57-7 2-mercapto-N-pentyl-nicotinamide 
• 330667-56-6 2-mercapto-N-propylnicotinamide 
• 91859-79-9 N-Benzyl-2-mercapto-nicotinamide 
• 154344-34-0 2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-46-4 2-(3-phenylpropyl)isothiazolo<5,4-b>pyridin-3(2H)-one 
• 154344-33-9 2-phenylethylisothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-45-3 2-phenethylisothiazolo<5,4-b>pyridin-3(2H)-one 
• 154344-32-8 2-benzylisothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-30-6 2-pentylisothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-43-1 2-pentylisothiazolo<5,4-b>pyridin-3(2H)-one 
• 154344-29-3 2-butylisothiazolo<5,4-b>pyridine-3(2H)-thione 

Downstream Products

• 154344-26-0 N-Benzyl-2-mercapto-thionicotinamide 
• 154344-28-2 2-Mercapto-N-(3-phenyl-propyl)-thionicotinamide 
• 154344-32-8 2-benzylisothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-33-9 2-phenylethylisothiazolo<5,4-b>pyridine-3(2H)-thione 
• 154344-27-1 2-Mercapto-N-phenethyl-thionicotinamide 
• 91859-79-9 N-Benzyl-2-mercapto-nicotinamide 
• 330667-58-8 2-mercapto-N-phenethyl-nicotinamide 
• 330667-59-9 2-mercapto-N-(3-phenyl-propyl)-nicotinamide 
• 65282-46-4 2-(p-chlorobenzyl)isothiazolo<5,4-b>pyridin-3-one 
• 65282-54-4 N-(p-chlorobenzyl)-2-mercaptonicotinamide 
• 65282-42-0 1,2-dithiolo<5,4-b>pyridin-3-one 

Relevant articles and documents

1,2-Dithiolan-3-ones and derivatives structurally related to leinamycin. Synthesis and biological evaluation

Leinamycin, an antitumor antibiotic isolated from Streptomyces sp., shows a 1,2-dithiolan-3-one 1-oxide heterocycle that appears to be involved in the biological activity. Several derivatives related to 1,2-dithiolan-3-one 1-oxide have been prepared and their activity as antineoplastic agents have been investigated. The synthesized compounds did not display a significative antitumor or cytotoxic activity in vitro.

Synthesis of 2-Substituted Isothiazolopyridin-3-ones

The synthesis of some 2-substituted derivatives 1-4 of all four isomeric isothiazolopyridin-3-ones is described.Several novel 1,2-dithiolopyridin-3-ones and 3-thiones were prepared as intermediates.