CAS 89481-98-1

Pyridine,2-chloro-6-(1-methylethoxy)-

Description:

Pyridine, 2-chloro-6-(1-methylethoxy)-, also known by its CAS number 89481-98-1, is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom and an ethoxy group. The presence of the chlorine atom at the 2-position and the 1-methylethoxy 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, and it is soluble in organic solvents. Pyridine derivatives are known for their applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. The presence of the chlorine atom can enhance reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the ethoxy group can influence the compound's polarity and solubility, affecting its behavior in different chemical environments. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₈H₁₀ClNO

Pyridine,2-chloro-6-(1-methylethoxy)-

CAS: 89481-98-1

Formula: C₈H₁₀ClNO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 171.6241

Ref: IN-DA00H4E4

2-Chloro-6-isopropoxypyridine

CAS: 89481-98-1

2-Chloro-6-isopropoxypyridine

Purity: ≥95%

Molecular weight: 171.62g/mol

Ref: 54-OR323114

2-Chloro-6-isopropoxypyridine

CAS: 89481-98-1

Purity: 98%

Molecular weight: 171.6199951

Ref: 10-F632286

2-Chloro-6-isopropoxypyridine

CAS: 89481-98-1

2-Chloro-6-isopropoxypyridine is a reactive organometallic compound that has the ability to form stable, structurally diverse, and often useful compounds. It can be used as an intermediate in the synthesis of substituted pyridines, furans, and other heterocycles. The synthesis of these compounds is usually achieved through cycloaddition reactions with suitably substituted arenes. 2-Chloro-6-isopropoxypyridine can be synthesized by the lithium chloride induced elimination reaction between chloroacetone and isopropyl alcohol at low temperatures. This method is regioselective, in that it gives a mixture of 2-chloro-6-isopropoxypyridine and its diastereoisomer.
2CIP produces a mixture of products with different substitution patterns because it undergoes a cycloaddition reaction with substituents on the aromatic ring. The lithiation

Formula: C₈H₁₀NOCl

Purity: Min. 95%

Molecular weight: 171.62 g/mol

Ref: 3D-PDA48198