Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
19892
CAS Number:
405933-97-3
2-(4-bromophényl)-4-chloro-6-méthyl-quinazoline
Documents
Available - Request Bulk Quote
Taille
Request Bulk Quote
Product Information

2-(4-Bromophenyl)-4-chloro-6-methyl-quinazoline is a versatile compound with significant potential in pharmaceutical research and development. This quinazoline derivative is recognized for its unique structural features, which contribute to its biological activity. It has been explored for its potential as an anti-cancer agent, particularly in targeting specific pathways involved in tumor growth and proliferation. Researchers appreciate its ability to serve as a scaffold for the development of novel therapeutic agents, making it a valuable tool in medicinal chemistry.

In addition to its applications in cancer research, 2-(4-Bromophenyl)-4-chloro-6-methyl-quinazoline has shown promise in the development of anti-inflammatory and antimicrobial agents. Its distinct properties allow for modifications that can enhance efficacy and selectivity, making it an attractive candidate for further investigation. The compound's stability and compatibility with various synthetic routes also facilitate its incorporation into complex chemical libraries, thereby accelerating the discovery of new drugs.

CAS Number
405933-97-3
Molecular Formula
C 15 H 10 BrClN 2
Molecular Weight
333.62
MDL Number
MFCD04115262
PubChem ID
53407512
Conditions
Conserver à 0-8°C
General Information
CAS Number
405933-97-3
Molecular Formula
C 15 H 10 BrClN 2
Molecular Weight
333.62
MDL Number
MFCD04115262
PubChem ID
53407512
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(4-Bromophenyl)-4-chloro-6-methyl-quinazoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting cancer and inflammatory diseases, enhancing drug efficacy.
  • Biological Research: It is used in studies exploring the mechanisms of action of quinazoline derivatives, contributing to the understanding of cellular processes and disease pathways.
  • Material Science: The compound finds applications in the development of novel materials, such as organic semiconductors, due to its unique electronic properties.
  • Analytical Chemistry: It acts as a reference standard in analytical methods, helping researchers ensure the accuracy and reliability of their experimental results.
  • Agrochemical Formulations: This chemical is explored for its potential use in developing agrochemicals, aimed at improving crop protection and yield.

Citations