CAS 168975-75-5

2-chloro-4-cyclopropylpyridine

Description:

2-Chloro-4-cyclopropylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with a chlorine atom at the second position and a cyclopropyl group at the fourth position. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure contributes to its unique chemical properties, including potential reactivity due to the presence of the chlorine atom, which can participate in nucleophilic substitution reactions. The cyclopropyl group introduces strain and can influence the compound's reactivity and stability. 2-Chloro-4-cyclopropylpyridine may be of interest in pharmaceutical research and development due to its potential biological activity, particularly in the context of drug design where pyridine derivatives are often explored for their pharmacological properties. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure proper safety measures are taken.

Formula: C₈H₈ClN

Synonyms:

• Pyridine, 2-chloro-4-cyclopropyl-
• 2-chloro-4-cyclopropylpyridine

Pyridine, 2-chloro-4-cyclopropyl-

CAS: 168975-75-5

Formula: C₈H₈ClN

Purity: 97%

Color and Shape: Liquid

Molecular weight: 153.6088

Ref: IN-DA001YES

2-Chloro-4-cyclopropylpyridine

CAS: 168975-75-5

2-Chloro-4-cyclopropylpyridine

Purity: 97%

Molecular weight: 153.61g/mol

Ref: 54-OR85213

2-Chloro-4-cyclopropylpyridine

CAS: 168975-75-5

Formula: C₈H₈ClN

Purity: 97%

Color and Shape: Liquid

Molecular weight: 153.61

Ref: 10-F497217

2-Chloro-4-cyclopropylpyridine

CAS: 168975-75-5

2-Chloro-4-cyclopropylpyridine is a chemical compound that contains a chlorine atom. It can be synthesized in the laboratory by condensing chloroacetic acid with cyclopropyl bromide, followed by hydrolysis of the ester group. This process can also be performed using sodium methoxide and chloride as reagents, or alternatively with sodium sulfate and diisopropyl phosphite. The salt form of this compound is soluble in water, whereas the free base is insoluble. 2-Chloro-4-cyclopropylpyridine has been used as a catalyst for the synthesis of tosylates from alcohols or phenols. It is primarily used in organic synthesis because it reacts efficiently with alcohols and phenols to produce tosylates without side reactions. 2-Chloro-4-cyclopropylpyridine also reacts with chlorine gas to produce dichlorocarbene, which

Formula: C₈H₈ClN

Purity: Min. 95%

Molecular weight: 153.61 g/mol

Ref: 3D-TGA97575