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Catalog Number:
25062
CAS Number:
122794-99-4
Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate
Purity:
≥ 98% (HPLC)
Synonym(s):
6-Bromo-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
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Product Information

Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate is a versatile compound with significant applications in pharmaceutical research and development. This compound is recognized for its unique structure, which includes a bromine atom and a hydroxyl group, making it a valuable intermediate in the synthesis of various bioactive molecules. Its ability to act as a building block in the development of quinoline derivatives positions it as a crucial component in the creation of potential therapeutic agents, particularly in the fields of antimicrobial and anticancer research.

Researchers have utilized Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate in the synthesis of novel compounds that exhibit promising biological activities. Its favorable properties, such as good solubility and stability, enhance its utility in laboratory settings. Additionally, the compound's unique reactivity allows for further modifications, enabling the exploration of new chemical entities with enhanced efficacy. This makes it an essential choice for professionals seeking to innovate in drug discovery and development.

Synonyms
6-Bromo-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
CAS Number
122794-99-4
Purity
≥ 98% (HPLC)
Molecular Formula
C12H10BrNO3
Molecular Weight
296.12
MDL Number
MFCD00173362
PubChem ID
689824
Melting Point
> 300 ?C
Appearance
Buff color powder
Conditions
Store at 0-8°C
General Information
Synonyms
6-Bromo-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
CAS Number
122794-99-4
Purity
≥ 98% (HPLC)
Molecular Formula
C12H10BrNO3
Molecular Weight
296.12
MDL Number
MFCD00173362
PubChem ID
689824
Melting Point
> 300 ?C
Appearance
Buff color powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial infections and other diseases, enhancing drug efficacy.
  • Biochemical Research: It is employed in studies related to enzyme inhibition and receptor binding, helping researchers understand biological pathways and develop new therapeutic strategies.
  • Material Science: The compound is used in the development of specialized coatings and polymers, providing enhanced durability and resistance to environmental factors.
  • Agricultural Chemistry: It finds applications in creating agrochemicals, such as fungicides and herbicides, contributing to improved crop protection and yield.
  • Analytical Chemistry: Ethyl 6-bromo-4-hydroxyquinoline-3-carboxylate is utilized as a reagent in various analytical techniques, aiding in the detection and quantification of other chemical substances.

Citations