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N'-benzyl-2-phenyl-acetohydrazide

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Identification
Molecular formula
C15H16N2O
CAS number
2904-41-4
IUPAC name
N'-benzyl-2-phenyl-acetohydrazide
State
State

At room temperature, N'-benzyl-2-phenyl-acetohydrazide is in a solid state. The typical form is a crystalline powder, indicating its stable state under ambient conditions.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
240.30g/mol
Molar mass
240.2940g/mol
Density
1.1030g/cm3
Appearence

N'-benzyl-2-phenyl-acetohydrazide is typically a white to off-white solid. The compound may form crystalline powders or aggregates, which are commonly observed in many organic compounds of this type.

Comment on solubility

Solubility of N'-benzyl-2-phenyl-acetohydrazide

N'-benzyl-2-phenyl-acetohydrazide is an intriguing compound whose solubility characteristics can be influenced by several factors. Generally, the solubility of organic compounds like this hydrazide is dependent on the following:

  • Polarity: Compounds with higher polarity tend to be more soluble in polar solvents, while nonpolar compounds prefer nonpolar solvents.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding can enhance solubility, especially in polar solvents.
  • Temperature: Increasing the temperature typically increases solubility, as it helps to overcome intermolecular forces.

For N'-benzyl-2-phenyl-acetohydrazide:

  • The compound likely exhibits moderate solubility in organic solvents such as ethanol, methanol, and DMSO.
  • It may have limited solubility in water due to its aromatic nature and relatively nonpolar characteristics.

In conclusion, while N'-benzyl-2-phenyl-acetohydrazide may not be highly soluble in water, its solubility in various organic solvents makes it versatile for different applications. As the saying goes, "Like dissolves like," emphasizing the significance of matching solvent polarity with the compound.

Interesting facts

Exploring N'-benzyl-2-phenyl-acetohydrazide

N'-benzyl-2-phenyl-acetohydrazide is a fascinating compound that belongs to the class of hydrazides, which play a significant role in organic synthesis and medicinal chemistry. Here are some intriguing points about this compound:

  • Multifunctional Applications: This compound has potential applications in drug discovery and development. Hydrazides are often considered for their biological activity, particularly in the design of new pharmaceuticals.
  • Complex Structure: The presence of both benzyl and phenyl groups in its structure contributes to its unique chemical properties, influencing its reactivity and interaction with biological systems.
  • Synthetic Versatility: N'-benzyl-2-phenyl-acetohydrazide can act as a versatile building block in organic synthesis, allowing chemists to create a variety of derivatives that could exhibit different chemical or biological properties.
  • Research Significance: Ongoing research into hydrazide compounds suggests that they may exhibit anti-inflammatory, anticancer, and antimicrobial activities, making them a subject of interest for medicinal chemists.
  • Functional Groups: The hydrazide functional group (–C(=O)NH–) is known for its ability to form a wide range of complexes with metal ions, enhancing its utility in coordination chemistry.

As with many compounds in organic chemistry, the study of N'-benzyl-2-phenyl-acetohydrazide not only expands our knowledge of hydrazides but also offers insights into their potential applications in various fields. This compound is indeed a key piece in the puzzle of chemical research!

Synonyms
ACETIC ACID, PHENYL-, 2-BENZYLHYDRAZIDE
1087-35-0
Benzeneacetic acid, 2-(phenylmethyl)hydrazide
GE4N2UQ9L1
NIOSH/AJ3257000
1-Benzyl-2-(benzylcarbonyl)hydrazine
NSC-58889
Phenylacetic acid 2-(phenylmethyl)hydrazide
Phenylacetic acid 2-(phenylmethylhydrazide)
AJ32570000
Acetic acid, phenyl-, 2-(phenylmethylhydrazide)
Phenylacetic acid 2-benzylhydrazide
N-Benzyl-N'-phenylacetylhydrazide
NSC 58889
BRN 0747771
P-5307
UNII-GE4N2UQ9L1
3-15-00-00704 (Beilstein Handbook Reference)
SCHEMBL8843411
DTXSID20148716
NSC58889