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Catalog Number:
25061
CAS Number:
70271-77-1
Ethyl 6-chloro-4-hydroxyquinoline-3-carboxylate
Purity:
≥ 98% (HPLC)
Synonym(s):
6-Chloro-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
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$132.20 /1G
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Product Information

Ethyl 6-chloro-4-hydroxyquinoline-3-carboxylate is a versatile compound recognized for its significant applications in pharmaceutical and agrochemical industries. This compound, also known as Ethyl 6-chloro-4-oxoquinoline-3-carboxylate, exhibits unique properties that make it valuable in the synthesis of various biologically active molecules. Its structural features allow it to act as a precursor in the development of antimicrobial agents and other therapeutic compounds, showcasing its potential in drug discovery and development.

In addition to its pharmaceutical relevance, Ethyl 6-chloro-4-hydroxyquinoline-3-carboxylate is also utilized in agricultural formulations, where it can contribute to the development of effective crop protection agents. Researchers appreciate its ability to enhance the efficacy of active ingredients, making it a sought-after compound in the formulation of pesticides and herbicides. Its stability and compatibility with various solvents further enhance its utility in diverse applications, making it an essential component for professionals in both research and industrial settings.

Synonyms
6-Chloro-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
CAS Number
70271-77-1
Purity
≥ 98% (HPLC)
Molecular Formula
C12H10ClNO3
Molecular Weight
251.67
MDL Number
MFCD00173342
PubChem ID
718113
Melting Point
> 300 ?C
Appearance
Off-white powder
Conditions
Store at 0-8°C
General Information
Synonyms
6-Chloro-4-hydroxy-3-quinolinecarboxylic acid ethyl ester
CAS Number
70271-77-1
Purity
≥ 98% (HPLC)
Molecular Formula
C12H10ClNO3
Molecular Weight
251.67
MDL Number
MFCD00173342
PubChem ID
718113
Melting Point
> 300 ?C
Appearance
Off-white 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-chloro-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 pharmaceutical agents, particularly those targeting bacterial infections, due to its antibacterial properties.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, helping to develop effective pesticides and herbicides that enhance crop protection against pests and diseases.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and receptor binding, aiding in the understanding of biochemical pathways and drug interactions.
  • Material Science: The compound is explored for its potential applications in creating novel materials, such as coatings or polymers, that require specific chemical properties for enhanced durability and performance.
  • Analytical Chemistry: It is utilized as a standard in various analytical techniques, such as chromatography, to ensure accurate measurement and validation of other compounds in complex mixtures.

Citations