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

Catalog Number:
17979
CAS Number:
730949-85-6
2-Chloromethyl-6,7-dimethoxy-3H-quinazolin-4-one
Purity:
≥ 95%
Synonym(s):
2-(Chloromethyl)-6,7-dimethoxyquinazolin-4(3H-one
Documents
$110.57 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

2-Chloromethyl-6,7-dimethoxy-3H-quinazolin-4-one is a versatile chemical compound recognized for its significant applications in medicinal chemistry and pharmaceutical research. This compound features a unique quinazolinone structure that enhances its potential as a building block for various bioactive molecules. Its chloromethyl and dimethoxy substituents contribute to its reactivity, making it an excellent candidate for further functionalization in drug development. Researchers have utilized this compound in the synthesis of novel therapeutic agents, particularly in the fields of oncology and neurology, where it has shown promise in targeting specific biological pathways.

The compound's unique properties allow for the development of derivatives that can exhibit improved efficacy and selectivity in biological systems. Its ability to serve as an intermediate in the synthesis of complex molecules makes it invaluable for researchers looking to innovate in drug design. With its favorable profile, 2-Chloromethyl-6,7-dimethoxy-3H-quinazolin-4-one stands out as a key ingredient in the quest for new therapeutic solutions.

Synonyms
2-(Chloromethyl)-6,7-dimethoxyquinazolin-4(3H-one
CAS Number
730949-85-6
Purity
≥ 95%
Molecular Formula
C11H11ClN2O3
Molecular Weight
254.67
MDL Number
MFCD04621482
PubChem ID
135473569
Appearance
Light grey powder
Boiling Point
~ 270 ?C (dec)
Conditions
Store at 0-8°C
General Information
Synonyms
2-(Chloromethyl)-6,7-dimethoxyquinazolin-4(3H-one
CAS Number
730949-85-6
Purity
≥ 95%
Molecular Formula
C11H11ClN2O3
Molecular Weight
254.67
MDL Number
MFCD04621482
PubChem ID
135473569
Appearance
Light grey powder
Boiling Point
~ 270 ?C (dec)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloromethyl-6,7-dimethoxy-3H-quinazolin-4-one is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceutical agents, particularly in the development of anti-cancer and anti-inflammatory drugs.
  • Biological Research: It is employed in studies investigating the mechanisms of action of quinazoline derivatives, aiding researchers in understanding their biological effects.
  • Material Science: The compound is used in creating novel materials with specific properties, such as enhanced thermal stability and electrical conductivity, beneficial for electronic applications.
  • Agricultural Chemistry: It finds applications in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that are safer for the environment.
  • Analytical Chemistry: This chemical is utilized as a standard in analytical methods, helping in the quantification and identification of similar compounds in complex mixtures.

Citations