CAS 77145-64-3

Pyridine, 2-chloro-6-(methylthio)-

Description:

Pyridine, 2-chloro-6-(methylthio)-, also known by its CAS number 77145-64-3, is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom and a methylthio group. The presence of the chlorine atom at the 2-position and the methylthio group at the 6-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid with a distinctive odor, reflecting the aromatic nature of the pyridine ring. It is soluble in organic solvents and exhibits moderate polarity. Pyridine derivatives, including this compound, are often utilized in various chemical syntheses and as intermediates in the production of agrochemicals, pharmaceuticals, and dyes. The chlorine substituent can enhance reactivity, making it a useful precursor for further chemical modifications. Additionally, the methylthio group can influence the compound's electronic properties and reactivity, potentially participating in nucleophilic substitution reactions. Safety precautions should be observed when handling this compound, as it may pose health risks upon exposure.

Formula: C₆H₆ClNS

Pyridine, 2-chloro-6-(methylthio)-

CAS: 77145-64-3

Formula: C₆H₆ClNS

Purity: 97%

Color and Shape: Liquid

Molecular weight: 159.6365

Ref: IN-DA005Q70

2-Chloro-6-(methylsulfanyl)pyridine

CAS: 77145-64-3

2-Chloro-6-(methylsulfanyl)pyridine

Purity: 95%

Molecular weight: 159.64g/mol

Ref: 54-OR32036

2-chloro-6-(methylthio)pyridine

CAS: 77145-64-3

Formula: C₆H₆ClNS

Purity: 98%

Color and Shape: Liquid

Molecular weight: 159.63

Ref: 10-F311320

2-Chloro-6-(methylsulfanyl)pyridine

CAS: 77145-64-3

2-Chloro-6-(methylsulfanyl)pyridine is an aromatic heterocyclic compound that contains a benzyl group and a pyridine ring. It has been used to synthesize 2,6-dichloropyrimidine nucleosides for the preparation of cytostatic drugs. This chemical compound has been shown to react with nucleophiles, such as hydroxide ion, through nucleophilic substitution reactions. This reaction is efficient and selective because the sulfinyl group can be removed by acid hydrolysis or hydrogenolysis and replaced with other functional groups. The pyridine ring is also unselective in these reactions because it can be reduced by lithium aluminum hydride to produce the corresponding amine.

Formula: C₆H₆ClNS

Purity: Min. 95%

Molecular weight: 159.64 g/mol

Ref: 3D-CDA14564