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Catalog Number:
24984
CAS Number:
27568-05-4
Ethyl 4-chloro-8-methoxyquinoline-3-carboxylate
Purity:
≥ 98% (HPLC)
Synonym(s):
4-Chloro-8-methoxyquinoline-3-carboxylic acid ethyl ester
Documents
$86.23 /250MG
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Product Information

Ethyl 4-chloro-8-methoxyquinoline-3-carboxylate is a versatile compound recognized for its significant applications in pharmaceutical research and development. This compound features a unique structure that enhances its potential as a building block in the synthesis of various bioactive molecules. Its chlorinated and methoxy-substituted quinoline framework is particularly valuable in the development of novel therapeutic agents, especially in the fields of anti-infective and anti-cancer drugs. Researchers have utilized this compound in the design of targeted therapies, leveraging its ability to interact with biological targets effectively.

In addition to its pharmaceutical applications, Ethyl 4-chloro-8-methoxyquinoline-3-carboxylate serves as a useful intermediate in organic synthesis, enabling the production of complex chemical entities. Its favorable reactivity profile and stability make it an attractive choice for chemists looking to streamline their synthesis processes. With its proven utility in medicinal chemistry and organic synthesis, this compound stands out as a valuable asset for researchers and industry professionals seeking innovative solutions in drug development and chemical manufacturing.

Synonyms
4-Chloro-8-methoxyquinoline-3-carboxylic acid ethyl ester
CAS Number
27568-05-4
Purity
≥ 98% (HPLC)
Molecular Formula
C13H12ClNO3
Molecular Weight
265.7
MDL Number
MFCD00173395
PubChem ID
304557
Melting Point
73-80 ?C
Appearance
Pale yellow amorphous powder
Conditions
Store at 0-8°C
General Information
Synonyms
4-Chloro-8-methoxyquinoline-3-carboxylic acid ethyl ester
CAS Number
27568-05-4
Purity
≥ 98% (HPLC)
Molecular Formula
C13H12ClNO3
Molecular Weight
265.7
MDL Number
MFCD00173395
PubChem ID
304557
Melting Point
73-80 ?C
Appearance
Pale yellow amorphous 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 4-chloro-8-methoxyquinoline-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 infectious diseases, due to its antibacterial and antifungal properties.
  • Biological Research: Researchers use it to study the mechanisms of action of quinoline derivatives, which can lead to the discovery of new therapeutic agents.
  • Agricultural Chemistry: It is applied in the formulation of agrochemicals, providing effective solutions for pest control while minimizing environmental impact compared to traditional pesticides.
  • Material Science: The compound is explored for its potential in developing advanced materials, such as coatings and polymers, that require specific chemical resistance and durability.
  • Analytical Chemistry: It is used as a standard reference material in analytical methods, helping ensure accuracy in the detection and quantification of related compounds in various samples.

Citations