CAS 7145-61-1
:3-chloro-6-(methylsulfanyl)pyridazine
Description:
3-Chloro-6-(methylsulfanyl)pyridazine is an organic compound characterized by its pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms. The presence of a chlorine atom at the 3-position and a methylsulfanyl group at the 6-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential reactivity due to the electrophilic nature of the chlorine atom and the nucleophilic character of the methylsulfanyl group. 3-Chloro-6-(methylsulfanyl)pyridazine may be of interest in various fields, including medicinal chemistry and agrochemicals, due to its potential biological activity and utility as a building block in synthetic pathways. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound exemplifies the diverse chemistry associated with substituted heterocycles.
Formula:C5H5ClN2S
InChI:InChI=1/C5H5ClN2S/c1-9-5-3-2-4(6)7-8-5/h2-3H,1H3
SMILES:CSc1ccc(Cl)nn1
Synonyms:- 3-Chloro-6-(methylthio)pyridazine
- Pyridazine, 3-chloro-6- (methylthio)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
3-Chloro-6-(methylthio)pyridazine
CAS:3-Chloro-6-(methylthio)pyridazinePurity:98%Molecular weight:160.63g/mol3-Chloro-6-(methylsulfanyl)pyridazine
CAS:<p>3-Chloro-6-(methylsulfanyl)pyridazine is a nucleophilic compound that is used as a reagent in organic synthesis. It can be used to form thiourea derivatives, which are nucleophilic and react with potassium to form potassium thiocyanate. 3-Chloro-6-(methylsulfanyl)pyridazine reacts with methanethiolate in the presence of nitrogen nucleophile to form 3-(methylthio)pyridine. This reaction can also be carried out with ethanethiolate, phenylmethanethiolate, or benzylmethanethiolate.>>END>></p>Formula:C5H5ClN2SPurity:Min. 95%Molecular weight:160.63 g/mol
