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Catalog Number:
19112
CAS Number:
92385-37-0
4-Amino-5-chloroquinoléine
Purity:
≥ 95 % (dosage)
Synonym(s):
5-Chloro-quinolin-4-ylamine
Documents
$470.00 /250 mg
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Product Information

4-Amino-5-chloroquinoline is a versatile chemical compound recognized for its significant applications in pharmaceuticals and research. This compound, a derivative of quinoline, exhibits notable antibacterial and antimalarial properties, making it a valuable asset in the development of therapeutic agents. Researchers have utilized 4-Amino-5-chloroquinoline in the synthesis of various bioactive molecules, particularly in the quest for new treatments against resistant strains of malaria and other infectious diseases. Its unique structure allows for modifications that enhance efficacy and reduce toxicity, which is crucial in drug development.

In addition to its medicinal applications, 4-Amino-5-chloroquinoline serves as an important intermediate in organic synthesis, facilitating the creation of complex chemical entities. Its relevance extends to the fields of materials science and agrochemicals, where it can be employed in the formulation of innovative products. The compound's stability and reactivity make it an ideal candidate for further exploration in diverse applications, ensuring that it remains a focal point for researchers and industry professionals alike.

Synonyms
5-Chloro-quinolin-4-ylamine
CAS Number
92385-37-0
Purity
≥ 95 % (dosage)
Molecular Formula
C9H7ClN2
Molecular Weight
178.62
MDL Number
MFCD06658303
PubChem ID
53408130
Appearance
Solide violet
Conditions
Conserver à 0-8°C
General Information
Synonyms
5-Chloro-quinolin-4-ylamine
CAS Number
92385-37-0
Purity
≥ 95 % (dosage)
Molecular Formula
C9H7ClN2
Molecular Weight
178.62
MDL Number
MFCD06658303
PubChem ID
53408130
Appearance
Solide violet
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Amino-5-chloroquinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various antimalarial and antibacterial agents, contributing to the fight against infectious diseases.
  • Biochemical Research: It is used in studies investigating the mechanisms of action of quinoline derivatives, helping researchers understand their effects on biological systems.
  • Analytical Chemistry: The compound is employed as a reagent in analytical techniques, such as chromatography, to detect and quantify specific substances in complex mixtures.
  • Material Science: 4-Amino-5-chloroquinoline is explored for its potential applications in developing novel materials, including polymers and coatings with enhanced properties.
  • Environmental Studies: Researchers utilize this chemical to assess its impact on ecosystems, particularly in studies related to pollution and its effects on aquatic life.

Citations