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Benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride

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Identification
Molecular formula
C16H20ClN4O2
CAS number
:null
IUPAC name
benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium;chloride
State
State

At room temperature, benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride is typically found as a solid.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.00
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.00
General information
Molecular weight
332.87g/mol
Molar mass
332.8650g/mol
Density
1.3200g/cm3
Appearence

The compound appears as a crystalline solid, typically white to off-white in color. Its appearance may vary slightly depending on the purity and specific preparation method used.

Comment on solubility

Solubility of Benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium Chloride

The solubility of benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride can be influenced by several factors, such as temperature and the solvent used. This compound exhibits characteristics typical of ionic compounds, given its ammonium chloride structure. To provide a clearer understanding of its solubility, consider the following points:

  • Temperature Effects: The solubility of many organic salts often increases with temperature. As temperature rises, the kinetic energy of the molecules increases, allowing more efficient interactions with solvent molecules.
  • Polar Solvents: This compound is likely to have good solubility in polar solvents, such as water and alcohols, due to its ionic nature. The chloride ion can interact favorably with polar solvents, enhancing solubility.
  • Hydrogen Bonding: The presence of functional groups, including the hydrazine and carbonyl moieties, can facilitate hydrogen bonding with solvent molecules, thereby improving solubility.
  • Practical Considerations: For practical applications, it is essential to perform solubility tests under varying conditions to determine the optimal environment for its dissolution.

In conclusion, while benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride has promising solubility characteristics in polar environments, further detailed studies may be required to quantify its solubility fully and explore its behavior in different solvents.

Interesting facts

Interesting Facts about Benzyl-[3-[2-(Pyridine-4-carbonyl)hydrazino]propanoyl]ammonium Chloride

Benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride, a fascinating compound, has garnered attention in various fields of study due to its diverse applications and unique chemical structure.

1. Structural Complexity

This compound features a hydrogen-bonding network owing to the presence of both the hydrazino and pyridine moieties, making it an interesting subject for structural analysis. Its intricate structure can lead to unique reactivity patterns, providing insights into:

  • Conformational chemistry
  • Hydrogen bonding interactions
  • Biological activity

2. Biological Significance

Compounds with similar structures to this benzyl derivative are frequently studied for their biological activities. Research suggests that:

  • Hydrazone derivatives often exhibit anticancer properties.
  • Pyridine-based compounds can act as enzyme inhibitors.
  • Quaternary ammonium groups have antimicrobial effects.

This means that the compound could hold potential therapeutic benefits in medicinal chemistry, particularly in drug design and development.

3. Synthesis and Applications

The synthesis of this compound typically integrates organic synthesis techniques, which may include:

  • Condensation reactions
  • Amidation processes
  • Various purification methods such as recrystallization

Such synthesis routes are not only essential for obtaining the compound but also serve educational purposes in organic chemistry labs.

4. Versatility in Research

From a research perspective, the compound’s ability to interact with different biological pathways can make it valuable for:

  • Studying drug-receptor interactions
  • Investigating disease mechanisms
  • Developing new therapeutic strategies

In summary, benzyl-[3-[2-(pyridine-4-carbonyl)hydrazino]propanoyl]ammonium chloride stands out as a compound of interest not only due to its complexity but also its potential in pharmaceutical research and organic synthesis.

Synonyms
Nialamide monohydrochloride
1161-03-1
Nialamide HCl
ISONICOTINIC ACID, 2-(2-(BENZYLCARBAMOYL)ETHYL)HYDRAZIDE, HYDROCHLORIDE