CAS 35740-86-4

2-bromo-3-methylquinoline

Description:

2-Bromo-3-methylquinoline is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the second position and a methyl group at the third position of the quinoline ring contributes to its unique chemical properties. This compound typically appears as a yellow to brown solid and is sparingly soluble in water but more soluble in organic solvents such as ethanol and dichloromethane. It exhibits notable reactivity due to the bromine substituent, which can participate in nucleophilic substitution reactions. Additionally, 2-bromo-3-methylquinoline can serve as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its derivatives may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that, like many brominated compounds, it should be handled with care due to potential toxicity and environmental concerns. Proper safety protocols should be followed when working with this substance in a laboratory setting.

Formula: C₁₀H₈BrN

InChI: InChI=1/C10H8BrN/c1-7-6-8-4-2-3-5-9(8)12-10(7)11/h2-6H,1H3

SMILES: Cc1cc2ccccc2nc1Br

Synonyms:

• 2-Bromo-3-methylquinoline
• Quinoline, 2-bromo-3-methyl-

2-Bromo-3-methylquinoline

CAS: 35740-86-4

Formula: C₁₀H₈BrN

Molecular weight: 222.0812

Ref: IN-DA00CB2I

2-Bromo-3-methylquinoline

CAS: 35740-86-4

2-Bromo-3-methylquinoline

Purity: ≥95%

Color and Shape: Solid

Molecular weight: 222.08g/mol

Ref: 54-OR300362

2-Bromo-3-methylquinoline

CAS: 35740-86-4

2-Bromo-3-methylquinoline is a pyrimidine compound that has been shown to have anti-inflammatory properties. It has been demonstrated to inhibit the conversion of propionate and acetyl-CoA into propionyl CoA, which is an important step in the synthesis of fatty acids. This inhibition leads to a decrease in the production of inflammatory leukotrienes and prostaglandins. 2-Bromo-3-methylquinoline also inhibits the formation of reactive oxygen species by inhibiting the conversion of isobutyrate into isobutyraldehyde, which results in decreased inflammation and oxidative stress.

Formula: C₁₀H₈BrN

Purity: Min. 95%

Molecular weight: 222.08 g/mol

Ref: 3D-KBA74086