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6-Bromo-2,8-dimethylquinoline-4-carboxylic acid

CAS 696620-11-8Formula C12H10BrNO2MW 280.12PubChem 1419046

This compound is a bromo-substituted quinoline carboxylic acid derivative, characterized by its quinoline core with bromo, methyl, and carboxylic acid functionalities. It is primarily intended for research and development applications.

Loading RDKit molecule structure...
InChIKey: DIXUJKRNHOZHIA-UHFFFAOYSA-NC12H10BrNO2 | MW 280.12

Chemical Identity

Molecular Formula

C12H10BrNO2

Molecular Weight

280.12 g/mol

Exact Mass

278.98949

PubChem CID

1419046

SMILES String

Cc1cc(C(=O)O)c2cc(Br)cc(C)c2n1

Names & Synonyms

6-Bromo-2,8-dimethyl-4-quinolinecarboxylic acid6-bromo-2,8-dimethyl-quinoline-4-carboxylic acid
External Identifiers
MFCD05260535SBB014125STK684369AKOS001743267ST4107888CS-0331322

Catalog Overview

6-Bromo-2,8-dimethylquinoline-4-carboxylic acid is an organic compound featuring a quinoline heterocyclic system. The quinoline ring is substituted with a bromine atom at position 6, two methyl groups at positions 2 and 8, and a carboxylic acid group at position 4. With a molecular formula of C12H10BrNO2 and a molecular weight of 280. 12, this compound falls into the "druglike_bioactive_like" structural bucket, suggesting its potential utility in medicinal chemistry research, medicinal chemistry research, or as a building block for synthesizing more complex molecules.

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

6-Bromo-2,8-dimethylquinoline-4-carboxylic acid is an organic compound featuring a quinoline heterocyclic system. The quinoline ring is substituted with a bromine atom at position 6, two methyl groups at positions 2 and 8, and a carboxylic acid group at position 4. With a molecular formula of C12H10BrNO2 and a molecular weight of 280.12, this compound falls into the "druglike_bioactive_like" structural bucket, suggesting its potential utility in medicinal chemistry research, medicinal chemistry research, or as a building block for synthesizing more complex molecules. Its distinct structural features make it a valuable tool for exploring structure-activity relationships and developing novel chemical entities in various research contexts.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white to off-white crystalline solid

Physical State

solid

Melting Point

220.0 °C

Density

1.5 g/cm³

Water Solubility

sparingly soluble

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle 6-Bromo-2,8-dimethylquinoline-4-carboxylic acid in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, away from incompatible materials.

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