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Catalog Number:
17756
CAS Number:
791626-58-9
6-Bromoquinolin-2-yl)amine
Purity:
≥ 97 % (HPLC)
Synonym(s):
2-Amino-6-bromoquinoléine, 6-Bromo-2-quinolinamine
Documents
$79.22 /250 mg
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Product Information

(6-Bromoquinolin-2-yl)amine is a versatile compound with significant applications in pharmaceutical research and development. This compound, characterized by its unique bromine substitution on the quinoline ring, serves as a valuable building block in the synthesis of various bioactive molecules. Its structural properties make it particularly relevant in the design of potential therapeutic agents targeting a range of diseases, including cancer and infectious diseases. Researchers have utilized (6-Bromoquinolin-2-yl)amine in the development of novel drug candidates, showcasing its ability to enhance biological activity and selectivity.

In addition to its pharmaceutical applications, (6-Bromoquinolin-2-yl)amine is also explored in material science and organic synthesis, where it can act as a ligand in coordination chemistry or as an intermediate in the production of functionalized quinoline derivatives. Its stability and reactivity make it an attractive option for researchers looking to innovate in various fields. With its broad applicability and potential for high-impact research, (6-Bromoquinolin-2-yl)amine stands out as a compound of interest for professionals aiming to advance their projects.

Synonyms
2-Amino-6-bromoquinoléine, 6-Bromo-2-quinolinamine
CAS Number
791626-58-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H7BrN2
Molecular Weight
223.07
MDL Number
MFCD06738670
PubChem ID
11183666
Melting Point
139-151 ?C
Appearance
Solide jaune à gris
Conditions
Conserver à 0-8 °C
General Information
Synonyms
2-Amino-6-bromoquinoléine, 6-Bromo-2-quinolinamine
CAS Number
791626-58-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C9H7BrN2
Molecular Weight
223.07
MDL Number
MFCD06738670
PubChem ID
11183666
Melting Point
139-151 ?C
Appearance
Solide jaune à gris
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

(6-Bromoquinolin-2-yl)amine is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceutical agents, particularly in developing anti-cancer and anti-inflammatory drugs.
  • Biological Research: Researchers use it to study its effects on cellular processes, helping to uncover mechanisms of action for potential therapeutic applications.
  • Fluorescent Probes: It is employed in creating fluorescent probes for bioimaging, allowing scientists to visualize cellular structures and processes in real-time.
  • Material Science: The compound is explored for its potential in developing new materials, including organic semiconductors, due to its unique electronic properties.
  • Environmental Monitoring: It can be used in the detection of pollutants, contributing to environmental safety and regulatory compliance in various industries.

Citations