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2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile

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Identification
Molecular formula
C12H10BrN3O
CAS number
76-70-2
IUPAC name
2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile
State
State

At room temperature, the compound is typically a solid. It is generally stable under recommended storage conditions.

Melting point (Celsius)
156.50
Melting point (Kelvin)
429.70
Boiling point (Celsius)
200.50
Boiling point (Kelvin)
473.70
General information
Molecular weight
275.12g/mol
Molar mass
275.1220g/mol
Density
1.5237g/cm3
Appearence

The compound is a solid that usually appears as powder or crystalline, and may have varied colors depending on its form.

Comment on solubility

Solubility of 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile

The solubility of 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile in various solvents is notably influenced by its chemical structure. Observations indicate:

  • Polarity: The presence of the ethoxy group contributes to intermediate polarity, which can lead to solubility in polar organic solvents.
  • Temperature Dependency: Like many organic compounds, solubility can increase with temperature, making warmer conditions beneficial for dissolution.
  • Solvent Specifics: This compound shows a general tendency to dissolve better in solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Acetone
    • Ethanol
  • Influence of Substituents: The presence of bromine and the ethoxy group may affect solubility due to their steric and electronic properties.

In summary, while 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile demonstrates potential solubility in various organic solvents, the extent of solubility will greatly depend on specific solvent interactions and temperature conditions.

Interesting facts

Interesting Facts about 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile

The compound 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile is a fascinating molecule that exemplifies the intricate nature of organic chemistry. Its complex structure and functional groups provide numerous insights into its potential applications and characteristics.

Key Features

  • Substituent Diversity: This compound features a **bromo** group, an **ethoxy** group, and a **dinitrile** moiety, demonstrating how varied substituents can influence the chemical properties and reactivity of the overall molecule.
  • Azo Linkage: The presence of an azo functional group is significant as it often incorporates vivid colors and is utilized in dyes. Additionally, azo compounds are known for their potential in solar energy conversion and photochemical reactions.
  • Biological Activity: Compounds like this one are often explored for their biological properties. The presence of the **bromo** substituent could enhance reactivity, making it a candidate for certain pharmaceutical applications.
  • Synthetic Pathways: Understanding how to synthesize such compounds expands the toolkit of chemists, allowing for the creation of a wide array of derivatives by altering substituents or reacting with other reagents.

Applications and Research Potential

Research into 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile has opened doors for numerous possibilities:

  • Materials Science: This compound could contribute to the development of new materials with unique electronic or optical properties.
  • Drug Development: Investigating its biological activity can lead to novel therapeutic agents, especially in the realm of antibacterial or anticancer research.
  • Environmental Chemistry: Its stability and reactivity make it a subject of interest in studies surrounding environmental impacts and degradation of similar compounds.

As you explore the world of organic compounds like 2-(2-bromo-4-ethoxy-phenyl)azopropanedinitrile, remember that every structure tells a story about interaction, reactivity, and the limitless potential within the field of chemistry!

Synonyms
((2-Bromo-4-ethoxyphenyl)azo)malononitrile
6017-35-2
F 2215
2-Brom-4-aethoxy-phenyl-azo-malonitril [German]
MALONONITRILE, ((2-BROMO-4-ETHOXYPHENYL)AZO)-
2-Brom-4-aethoxy-phenyl-azo-malonitril