CAS 63136-60-7

4-chloro-3-methylquinoline

Description:

4-Chloro-3-methylquinoline is an organic compound belonging to the quinoline family, characterized by a bicyclic structure that consists of a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 4-position and a methyl group at the 3-position of the quinoline structure, which influences its chemical reactivity and physical properties. It typically appears as a yellow to brown solid and is sparingly soluble in water but more soluble in organic solvents. The presence of the chlorine substituent can enhance its biological activity, making it of interest in medicinal chemistry and research. 4-Chloro-3-methylquinoline may exhibit various properties such as fluorescence and can participate in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the chlorine atom. Additionally, it may serve as a precursor or intermediate in the synthesis of other chemical compounds, including pharmaceuticals and agrochemicals. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled.

Formula: C₁₀H₈ClN

InChI: InChI=1/C10H8ClN/c1-7-6-12-9-5-3-2-4-8(9)10(7)11/h2-6H,1H3

SMILES: Cc1cnc2ccccc2c1Cl

Synonyms:

• 63136-60-7
• Quinoline, 4-chloro-3-methyl-
• T66 Bnj D1 Eg [Wln]

4-chloro-3-methylquinoline

CAS: 63136-60-7

Formula: C₁₀H₈ClN

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.6302

Ref: IN-DA003L52

4-Chloro-3-methylquinoline

CAS: 63136-60-7

4-Chloro-3-methylquinoline

Purity: 97%

Molecular weight: 177.63g/mol

Ref: 54-OR951626

4-Chloro-3-methylquinoline

CAS: 63136-60-7

Formula: C₁₀H₈ClN

Purity: 98%

Color and Shape: Solid

Molecular weight: 177.63

Ref: 10-F321281

4-Chloro-3-methylquinoline

CAS: 63136-60-7

4-Chloro-3-methylquinoline is an intramolecular reaction that is catalyzed by a strong base. It is a reagent that reacts with azide to form the cyclized product. The mechanism of this reaction proceeds in two steps. In the first step, the methyleniminium cation intermediate is formed by intramolecular cyclization. This intermediate then reacts with the azide ion to form the desired product. 4-Chloro-3-methylquinoline can also be used as a sterically demanding methylene group when it undergoes electrophilic substitution reactions with alkyl halides and other nucleophiles.

Formula: C₁₀H₈ClN

Purity: Min. 95%

Molecular weight: 177.63 g/mol

Ref: 3D-NCA13660