3-Chloro-5-methoxypyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a chlorine atom at the 3-position and a methoxy group (-OCH3) at the 5-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents, such as ethanol and dichloromethane, but has limited solubility in water due to the hydrophobic nature of the methoxy group and the aromatic structure. 3-Chloro-5-methoxypyridine is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, owing to its reactivity and ability to undergo various chemical transformations, including nucleophilic substitutions and coupling reactions. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used.

3-CHLORO-5-METHOXYPYRIDINE

95881-83-7: Pyridine, 3-Chloro-5-Methoxy-

3-Chloro-5-methoxypyridine (3CMP) is a nitrated organic compound that is synthesized by the nitration of 3-chloropyridine. The reaction involves the replacement of the hydrogen atom on the nitrogen atom with a chlorine atom, and it can be done in two ways: either by reacting with an acidified mixture of sulfuric and nitric acid, or by reacting with concentrated nitric acid. 3CMP has been used in research to study the reaction between substituted amines and hydroxylamine. In this reaction, 3CMP is used as a base to hydrolyze the substituent on the amine molecule to form an n-oxide.

CAS 95881-83-7: 3-CHLORO-5-METHOXYPYRIDINE

3-Chloro-5-methoxypyridine

Ref: 3D-FC148708

3-Chloro-5-methoxypyridine

Ref: 10-F236947

3-Chloro-5-methoxypyridine

Ref: IN-DA005WY6

3-Chloro-5-methoxypyridine

Ref: 54-OR952205

3-Chloro-5-methoxypyridine

Ref: FT-C34093