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Cinnamohydrazide

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Identification
Molecular formula
C9H10N2O
CAS number
621-32-9
IUPAC name
3-phenylprop-2-enehydrazide
State
State

At room temperature, cinnamohydrazide is in a solid state.

Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
148.17g/mol
Molar mass
148.1720g/mol
Density
1.0895g/cm3
Appearence

Cinnamohydrazide appears as a white to off-white crystalline powder. It is typically free-flowing with no significant odor.

Comment on solubility

Solubility of 3-phenylprop-2-enehydrazide

3-phenylprop-2-enehydrazide, a compound with a unique structure, exhibits specific solubility characteristics that can significantly influence its applications in various fields. Understanding its solubility behavior is essential for practical usage. The solubility of this compound can be summarized as follows:

  • Polar solvents: Generally, 3-phenylprop-2-enehydrazide shows moderate solubility in polar solvents like methanol and ethanol due to the presence of the hydrazide functional group.
  • Nonpolar solvents: In non-polar solvents such as hexane or chloroform, its solubility is typically low, reflecting its structural characteristics.
  • Influence of temperature: The solubility tends to increase with rising temperature, making it beneficial in scenarios where higher solubility is required for reactions or processes.
  • pH influence: As with many hydrazides, the solubility can be pH-dependent; under more acidic or basic conditions, alterations in solubility may occur due to ionization.

Overall, the solubility of 3-phenylprop-2-enehydrazide showcases an intricate balance, being more soluble in certain conditions while facing limitations in others. Understanding these nuances assists in effective usage in both industrial and laboratory settings.

Interesting facts

Interesting Facts about 3-phenylprop-2-enehydrazide

3-phenylprop-2-enehydrazide is a fascinating organic compound that has attracted interest in various fields of chemistry due to its versatile properties and potential applications. Here are some engaging highlights:

  • Structural Diversity: This compound features a hydrazide functional group, which is a nitrogen-containing group that can engage in various chemical reactions. This enables the formation of numerous derivatives, expanding its utility in synthesis.
  • Biological Relevance: Compounds containing hydrazide groups often exhibit significant biological activities, including anti-inflammatory, antimicrobial, and antitumor properties. Research into derivatives of 3-phenylprop-2-enehydrazide may yield compounds of pharmaceutical interest.
  • Reaction Versatility: This compound can participate in several types of chemical reactions, such as condensation and hydrazone formation. This versatility makes it a valuable intermediate in organic synthesis.
  • Applications in Material Science: In certain formulations, hydrazide groups can improve the mechanical properties of polymers and potentially enhance the performance of composite materials.
  • Analytical Techniques: 3-phenylprop-2-enehydrazide can be analyzed using techniques like NMR (Nuclear Magnetic Resonance) and IR (Infrared Spectroscopy), providing insight into its structure and confirmations.

As a compound with a hydrazide moiety and a phenyl group, 3-phenylprop-2-enehydrazide exemplifies the intricate relationship between structure and reactivity in organic chemistry. Its diverse applications make it a compound of ongoing interest for researchers and industry alike.

In the words of a renowned chemist: "The beauty of organic compounds lies in their ability to transform and adapt, providing endless opportunities for discovery."

Synonyms
cinnamic acid hydrazide
3-Phenyl-2-propenoic acid hydrazide
DTXSID501294768
DS-014345