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Catalog Number:
20265
CAS Number:
885277-29-2
4-Chloro-2-(4-methoxyphenyl)-5-methyl-quinazoline
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Product Information

4-Chloro-2-(4-methoxyphenyl)-5-methyl-quinazoline is a versatile compound known for its significant applications in pharmaceutical research and development. This quinazoline derivative exhibits promising biological activities, making it a valuable candidate for the synthesis of novel therapeutic agents. Its unique structure allows for potential use in the development of anti-cancer drugs, as well as in treatments targeting various diseases due to its ability to interact with specific biological pathways. Researchers have noted its effectiveness in inhibiting certain enzymes, which can be pivotal in drug design and discovery processes.

In addition to its pharmaceutical applications, 4-Chloro-2-(4-methoxyphenyl)-5-methyl-quinazoline can also serve as a key intermediate in organic synthesis, providing a foundation for the development of more complex molecules. Its favorable properties, such as stability and reactivity, make it an attractive option for chemists looking to innovate in medicinal chemistry and related fields. With its potential to enhance drug efficacy and broaden therapeutic options, this compound stands out as a significant asset in both research and industrial applications.

CAS Number
885277-29-2
Molecular Formula
C16H13ClN2O
Molecular Weight
284.75
MDL Number
MFCD04115238
PubChem ID
53407923
Conditions
Store at 0-8°C
General Information
CAS Number
885277-29-2
Molecular Formula
C16H13ClN2O
Molecular Weight
284.75
MDL Number
MFCD04115238
PubChem ID
53407923
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

4-Chloro-2-(4-methoxyphenyl)-5-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 investigating the mechanisms of action of quinazoline derivatives, contributing to the understanding of their biological activities and potential therapeutic effects.
  • Agricultural Chemistry: The compound can be explored for its potential as a pesticide or herbicide, offering an innovative approach to crop protection with reduced environmental impact.
  • Material Science: It finds applications in developing new materials, particularly in the creation of organic semiconductors, which are essential for advanced electronic devices.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting and quantifying quinazoline derivatives in various samples, aiding quality control in pharmaceutical manufacturing.

Citations