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4-Fluoro-N'-phenylbenzohydrazide

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Identification
Molecular formula
C13H11FN2O
CAS number
13429-12-8
IUPAC name
4-fluoro-N'-phenyl-benzohydrazide
State
State
Solid at room temperature, typically in a crystalline form.
Melting point (Celsius)
158.50
Melting point (Kelvin)
431.65
Boiling point (Celsius)
373.10
Boiling point (Kelvin)
646.25
General information
Molecular weight
230.23g/mol
Molar mass
230.2310g/mol
Density
1.2590g/cm3
Appearence

4-Fluoro-N'-phenylbenzohydrazide appears as a white to off-white crystalline powder. It is usually handled in its solid form and has a fine crystalline texture.

Comment on solubility

Solubility of 4-fluoro-N'-phenyl-benzohydrazide

4-fluoro-N'-phenyl-benzohydrazide exhibits some intriguing properties when it comes to solubility.

Solvent Interaction

This compound demonstrates variable solubility depending on the solvent used. In general, it is:

  • Slightly soluble in polar solvents like water, due to the presence of polar functional groups.
  • More soluble in organic solvents, such as ethanol and acetone, which can effectively solvate the hydrazide group.

Effect of Temperature

As a general rule, increasing the temperature can enhance the solubility of 4-fluoro-N'-phenyl-benzohydrazide in organic solvents. An increase in molecular kinetic energy often leads to increased solvation interactions.

Factors Influencing Solubility

Several factors can influence the solubility of this compound:

  • Polarity: The more polar the solvent, the better the chances of solubility for compounds like this one that have polar functional groups.
  • Hydrogen Bonding: The ability of 4-fluoro-N'-phenyl-benzohydrazide to form hydrogen bonds with solvents can significantly affect its solubility.
  • Concentration: At higher concentrations, solubility may also decrease due to saturation effects.

In summary, while 4-fluoro-N'-phenyl-benzohydrazide is not highly soluble in water, it demonstrates appreciable solubility in various organic solvents, making it versatile for different chemical applications.

Interesting facts

Interesting Facts about 4-fluoro-N'-phenyl-benzohydrazide

4-fluoro-N'-phenyl-benzohydrazide is a fascinating compound that has garnered interest in various fields of research, particularly in medicinal chemistry. Here are some engaging insights into this intriguing compound:

  • Potent Biological Activity: This compound exhibits significant biological properties, making it a candidate for further pharmacological studies. Its potential use includes exploring its role as a therapeutic agent against several diseases.
  • Structure-Activity Relationship (SAR): The incorporation of the 4-fluoro group is essential. Fluorine substitutions often enhance the lipophilicity and metabolic stability of drug candidates, thus influencing their pharmacokinetics.
  • Chemical Versatility: 4-fluoro-N'-phenyl-benzohydrazide can serve as a building block for the synthesis of more complex molecules, supporting advancements in drug discovery and development.
  • Research Applications: This compound is frequently utilized in the synthesis of various derivatives that could lead to more potent agents in the fight against diseases such as cancer or bacterial infections.
  • Hydrazone Chemistry: Being part of the hydrazide functional group, it may partake in important hydrazone formation reactions, which are vital in both organic synthesis and biochemical pathways.
  • Impact of Fluorine: The presence of fluorine in organic compounds not only affects their reactivity and stability but also enhances their bioavailability, which is a critical factor in drug design.

In summary, 4-fluoro-N'-phenyl-benzohydrazide represents a compelling intersection of structure, functionality, and biological activity, making it a compound of interest for future explorations in various scientific avenues.

Synonyms
4-fluoro-N'-phenylbenzohydrazide
1496-02-2
BENZOIC ACID, p-FLUORO-, 2-PHENYLHYDRAZIDE
p-Fluorobenzoic acid 2-phenylhydrazide
BRN 0959317
SCHEMBL9829474
DTXSID80164351
PGKDUKIHKGXXIY-UHFFFAOYSA-N
AKOS003791963
4-Fluorobenzoic acid, 2-phenylhydrazide
4-Fluorobenzoic acid-N'-phenylhydrazide