CAS 201420-31-7

6-Bromo-4-chloro-3-quinolinecarboxaldehyde

Description:

6-Bromo-4-chloro-3-quinolinecarboxaldehyde is an organic compound characterized by its quinoline structure, which is a bicyclic aromatic compound containing a nitrogen atom. This substance features a carboxaldehyde functional group, which is indicative of its reactivity and potential applications in organic synthesis. The presence of bromine and chlorine substituents on the quinoline ring enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The compound is typically used in the synthesis of more complex molecules, particularly in medicinal chemistry and material science. Its unique structure allows for potential interactions with biological targets, making it of interest in drug development. Additionally, the compound may exhibit specific physical properties such as solubility in organic solvents and distinct spectral characteristics in techniques like NMR and IR spectroscopy. Safety and handling precautions should be observed due to the presence of halogenated groups, which can pose environmental and health risks.

Formula: C₁₀H₅BrClNO

InChI: InChI=1S/C10H5BrClNO/c11-7-1-2-9-8(3-7)10(12)6(5-14)4-13-9/h1-5H

InChI key: InChIKey=SJSGLHNBLBNADM-UHFFFAOYSA-N

SMILES: ClC=1C2=C(N=CC1C=O)C=CC(Br)=C2

Synonyms:

• 3-Quinolinecarboxaldehyde, 6-bromo-4-chloro-
• 6-Bromo-4-chloro-3-quinolinecarboxaldehyde

3-Quinolinecarboxaldehyde, 6-bromo-4-chloro-

CAS: 201420-31-7

Formula: C₁₀H₅BrClNO

Purity: 96%

Color and Shape: Solid

Molecular weight: 270.5098

Ref: IN-DA002DED

6-Bromo-4-chloroquinoline-3-carbaldehyde

CAS: 201420-31-7

6-Bromo-4-chloroquinoline-3-carbaldehyde

Purity: 95%

Molecular weight: 270.51g/mol

Ref: 54-OR78681

6-Bromo-4-chloroquinoline-3-carbaldehyde

CAS: 201420-31-7

Formula: C₁₀H₅BrClNO

Purity: 96%

Molecular weight: 270.51

Ref: 10-F321773