1391268-61-3

Basic information

• Product Name: 5-broMo-2,3-dihydroquinolin-4(1H)-one
• Synonyms: 5-broMo-2,3-dihydroquinolin-4(1H)-one
• CAS NO: 1391268-61-3
• Molecular Formula: C9H8BrNO
• Molecular Weight: 226.06992
• Mol File: 1391268-61-3.mol

Chemical Properties

• Boiling Point: 357.7±42.0 °C(Predicted)
• Appearance: /
• Density: 1.559±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C(protect from light)
• PKA: 1.65±0.20(Predicted)
• CAS DataBase Reference: 5-broMo-2,3-dihydroquinolin-4(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-broMo-2,3-dihydroquinolin-4(1H)-one(1391268-61-3)
• EPA Substance Registry System: 5-broMo-2,3-dihydroquinolin-4(1H)-one(1391268-61-3)

Safety Data

• Hazardous Substances Data: 1391268-61-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-Bromo-2,3-dihydroquinolin-4(1H)-one is used as an intermediate in organic synthesis for the preparation of various chemical compounds. Its unique structure allows for further functionalization and modification, making it a versatile building block in the synthesis of complex organic molecules.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Bromo-2,3-dihydroquinolin-4(1H)-one is used as a starting material for the development of new pharmaceutical drugs. Its potential pharmacological properties, such as anti-tumor and anti-inflammatory activities, make it a promising candidate for drug discovery and optimization.
Used in Antitumor Applications:
5-Bromo-2,3-dihydroquinolin-4(1H)-one is used as an anti-tumor agent for its potential to inhibit the growth and proliferation of cancer cells. Its mechanism of action may involve targeting specific cellular pathways or enzymes involved in tumor development and progression, making it a valuable tool in cancer research and treatment.
Used in Anti-inflammatory Applications:
5-Bromo-2,3-dihydroquinolin-4(1H)-one is also used as an anti-inflammatory agent, potentially reducing inflammation and associated symptoms in various diseases and conditions. Its anti-inflammatory properties may be attributed to its ability to modulate immune responses or inhibit the production of inflammatory mediators.
Used in Precursor for Bioactive Compounds:
5-Bromo-2,3-dihydroquinolin-4(1H)-one serves as a precursor for the synthesis of bioactive compounds with potential therapeutic applications. Its unique structure and functional groups can be utilized to create new molecules with enhanced biological activities, contributing to the development of novel pharmaceuticals and therapeutic agents.
Used in Development of New Materials and Chemical Processes:
Furthermore, 5-Bromo-2,3-dihydroquinolin-4(1H)-one may have applications in the development of new materials and chemical processes. Its chemical properties and reactivity can be harnessed to create innovative materials with unique properties or to improve existing chemical processes in various industries.