35101-71-4

Basic information

• Product Name: 11-bromo-11H-indeno[1,2-b]quinoxaline
• CAS NO: 35101-71-4
• Molecular Formula: C₁₅H₉BrN₂
• Molecular Weight: 297.1494
• Mol File: 35101-71-4.mol

Chemical Properties

• Boiling Point: 442.2°C at 760 mmHg
• Flash Point: 221.2°C
• Density: 1.621g/cm³
• Vapor Pressure: 1.33E-07mmHg at 25°C
• Refractive Index: 1.762
• CAS DataBase Reference: 11-bromo-11H-indeno[1,2-b]quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 11-bromo-11H-indeno[1,2-b]quinoxaline(35101-71-4)
• EPA Substance Registry System: 11-bromo-11H-indeno[1,2-b]quinoxaline(35101-71-4)

Safety Data

• Hazardous Substances Data: 35101-71-4(Hazardous Substances Data)

Usage

Structure

Heterocyclic compound with an indenoquinoline core and a bromine atom at position 11
The compound features a complex ring structure with a bromine atom attached to the 11th position of the indenoquinoline core.

Field of application

Organic and medicinal chemistry
It is used in the development of pharmaceutical drugs and has potential therapeutic applications.

Biological activities

Anti-tumor and anti-inflammatory properties
The compound has been studied for its ability to inhibit tumor growth and reduce inflammation.

Potential use

Building block for the synthesis of various organic compounds
Due to its unique molecular structure, it can be used as a starting material for the synthesis of other organic compounds.

Chemical properties

Reactivity with other compounds
The presence of the bromine atom at position 11 may allow for further chemical reactions and modifications, such as substitution or addition reactions.

Physical properties

Appearance, solubility, and stability
The compound's appearance, solubility in various solvents, and stability under different conditions are important factors to consider for its practical applications.

Synthesis methods

Various synthetic routes to obtain the compound
The compound can be synthesized through different chemical reactions and pathways, which may involve the formation of the indenoquinoline core and subsequent bromination.

Purification techniques

Methods to isolate and purify the compound
Techniques such as recrystallization, chromatography, or distillation may be employed to obtain a pure sample of the compound.

Safety and handling

Precautions and guidelines for safe handling and storage
As with any chemical compound, it is essential to follow proper safety protocols, including the use of personal protective equipment and proper storage conditions.

Environmental impact

Potential effects on the environment and guidelines for disposal
The compound's environmental impact should be considered, and appropriate disposal methods should be followed to minimize any negative effects.