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Catalog Number:
17772
CAS Number:
65340-75-2
4-Amino-8-bromoquinolina
Purity:
≥ 95 % (HPLC)
Synonym(s):
8-Bromo-quinolin-4-ilamina
Documents
$96.34 /250 mg
Tamaño
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Product Information

4-Amino-8-bromoquinoline is a versatile compound recognized for its significant role in pharmaceutical and chemical research. This compound, characterized by its unique bromine and amino functional groups, serves as a crucial building block in the synthesis of various bioactive molecules. Its structure allows for diverse modifications, making it an essential intermediate in the development of novel drugs, particularly in the fields of anti-infective and anti-cancer therapies. Researchers have utilized 4-Amino-8-bromoquinoline in the synthesis of quinoline derivatives, which are known for their biological activities, including antimicrobial and antimalarial properties.

In addition to its pharmaceutical applications, this compound is also valuable in materials science, where it can be employed in the development of organic semiconductors and dyes. Its ability to act as a ligand in coordination chemistry further enhances its utility in catalysis and sensor technology. With its broad range of applications, 4-Amino-8-bromoquinoline stands out as a compound of interest for both academic research and industrial applications, offering unique advantages in the synthesis of complex molecules and materials.

Synonyms
8-Bromo-quinolin-4-ilamina
CAS Number
65340-75-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H7BrN2
Molecular Weight
223.07
MDL Number
MFCD04037193
PubChem ID
12403693
Melting Point
190-196 ?C
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
8-Bromo-quinolin-4-ilamina
CAS Number
65340-75-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C9H7BrN2
Molecular Weight
223.07
MDL Number
MFCD04037193
PubChem ID
12403693
Melting Point
190-196 ?C
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Amino-8-bromoquinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of antimalarial and anticancer agents.
  • Biological Research: It is employed in studies investigating the mechanisms of action of quinoline derivatives, helping researchers understand their biological activities and potential therapeutic effects.
  • Material Science: The compound is used in the formulation of organic electronic materials, contributing to advancements in organic light-emitting diodes (OLEDs) and organic photovoltaics.
  • Analytical Chemistry: It acts as a reagent in analytical methods for detecting and quantifying specific biomolecules, enhancing the accuracy of various assays.
  • Environmental Monitoring: 4-Amino-8-bromoquinoline is utilized in the detection of pollutants, aiding in the assessment of environmental samples for harmful substances.

Citas