479628-47-2

Basic information

• Product Name: 3-chloro-6-(1-ethoxyvinyl)pyridazine
• Synonyms: 3-chloro-6-(1-ethoxyvinyl)pyridazine
• CAS NO: 479628-47-2
• Molecular Weight: 184.625
• Mol File: 479628-47-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-chloro-6-(1-ethoxyvinyl)pyridazine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-6-(1-ethoxyvinyl)pyridazine(479628-47-2)
• EPA Substance Registry System: 3-chloro-6-(1-ethoxyvinyl)pyridazine(479628-47-2)

Safety Data

• Hazardous Substances Data: 479628-47-2(Hazardous Substances Data)

Upstream product

• 141-30-0 3,6-dichlorpyridazine 
• 97674-02-7 tributyl(1-ethoxyvinyl)stannane 

Relevant articles and documents

SUBSTITUTED N-(METHYL-D3)PYRIDAZINE-3-CARBOXAMIDE OR N-(METHYL-D3)-NICOTINAMIDE COMPOUNDS AS IL-12, IL-23 AND/OR IFNALPHA MODULATORS

There are disclosed compounds of the following formula I or a stereoisomer or pharmaceutically-acceptable salt thereof, wherein all substituents are as defined herein, which are useful in the modulation of IL-12, IL-23 and/or IFN?, by acting on Tyk-2 to cause signal transduction inhibition. The compounds of the invention may be useful for treating inflammatory and autoimmune diseases or disorders.

Hepatitis C Virus Inhibitors

The present disclosure relates to compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

Helical self-organization and hierarchical self-assembly of an oligoheterocyclic pyridine-pyridazine strand into extended supramolecular fibers

The synthesis and characterization of an alternating pyridine-pyridazine strand comprising thirteen heterocycles are described. Spontaneous folding into a helical secondary structure is based on a general molecular self-organization process enforced by the conformational information encoded within the primary structure of the molecular strand itself. Conformational control based on heterocyclic helicity codons illustrates a strategy for designing folding properties into synthetic oligomers (foldamers). Strong intermolecular interactions of the highly ordered lock-washer subunits of compound 3 results in hierarchical supramolecular self-assembly into protofibrils and fibrils. Compound 3 also forms mechanically stable two-dimensional Langmuir-Blodgett and cast thin films.