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N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide

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Identification
Molecular formula
C15H17N3O
CAS number
21240-57-9
IUPAC name
N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide
State
State

At room temperature, N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide is typically found in a solid state. It is stable under normal environmental conditions.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
465.00
Boiling point (Kelvin)
738.15
General information
Molecular weight
265.33g/mol
Molar mass
265.3250g/mol
Density
1.1750g/cm3
Appearence

This compound typically appears as a crystalline solid. Its color ranges from white to off-white, depending on the exact purity and conditions of synthesis.

Comment on solubility

Solubility of N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide

N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide is a compound that presents intriguing solubility characteristics. Understanding its solubility can provide insight into its potential applications and behavior in various environments. Here are some noteworthy points regarding its solubility:

  • Polar and Non-polar Interactions: The structure of this compound includes both polar (the pyridine and hydrazide components) and non-polar sections (the phenyl and methyl groups), which suggests that it may exhibit moderate solubility in both polar and non-polar solvents.
  • Solvent Compatibility: This compound would likely dissolve better in solvents such as dimethyl sulfoxide (DMSO) or ethanol, where the polar portion can interact favorably with the solvent molecules.
  • Temperature Dependence: Like many organic compounds, the solubility of N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide can vary significantly with temperature, potentially increasing at elevated temperatures due to enhanced molecular motion.
  • pH Influence: The solubility might also be influenced by the pH of the solution, as the hydrazide moiety can participate in acid-base reactions that alter the compound's ionization state and, consequently, its solubility.

In summary, the solubility of N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide is expected to be relatively versatile, with variables such as polarity, temperature, and pH playing crucial roles in determining the extent to which it can dissolve in different environments.

Interesting facts

Exploring N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide

N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide is a unique and fascinating compound that draws attention for its diverse applications and complex structure. Here are some interesting facts about this intriguing molecule:

  • Medicinal Chemistry: This compound has potential applications in medicinal chemistry, where the incorporation of heterocyclic rings like pyridine can enhance biological activity.
  • Synthesis: The synthesis of this compound can involve a variety of methodologies, including hydrazone formation, which is a popular reaction in organic chemistry for generating hydrazides from carbonyl compounds.
  • Chemical Reactivity: The presence of both pyridine and hydrazide functionalities provides a rich chemistry that can lead to various derivatives with altered properties, potentially impacting their pharmacological profiles.
  • Structure-Activity Relationship (SAR): Studying the relationship between its structure and biological activity can unveil significant insights, showing how structural modifications can lead to enhanced efficacy.
  • Multifunctionality: Compounds like this often exhibit multifunctionality, meaning they can engage in multiple types of chemical interactions, which can be harnessed in drug design and development.

As researchers continue to explore the vast world of organic compounds, the study of N'-(1-methyl-2-phenyl-ethyl)pyridine-2-carbohydrazide exemplifies the intricate dance between molecular structure and function. Its significance in the realms of chemistry and biology reminds us that even a single compound can hold a wealth of possibilities and scientific intrigue.