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N-Benzylidene-N'-benzylguanidine

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Identification
Molecular formula
C15H15N3
CAS number
32042-11-0
IUPAC name
2-benzyl-1-(benzylideneamino)guanidine
State
State

At room temperature, N-Benzylidene-N'-benzylguanidine is a solid. Typically, it is in a crystalline state and remains stable under standard conditions of temperature and pressure.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
312.00
Boiling point (Kelvin)
585.15
General information
Molecular weight
252.32g/mol
Molar mass
252.3150g/mol
Density
1.2000g/cm3
Appearence

N-Benzylidene-N'-benzylguanidine typically appears as a crystalline solid. The color may range from off-white to pale yellow, depending on the purity and specific form. The crystals are usually well-formed with sharp edges.

Comment on solubility

Solubility of 2-benzyl-1-(benzylideneamino)guanidine

The solubility of 2-benzyl-1-(benzylideneamino)guanidine is an intriguing aspect that can influence its applications in various fields. Here are some key points to consider:

  • Nature of the Compound: The presence of multiple functional groups, including the guanidine group, plays a significant role in its solubility characteristics.
  • Polarity: The overall polarity of the molecule affects how it interacts with solvents. Compounds with more polar functional groups tend to have higher solubility in polar solvents such as water.
  • Solvent Preferences: It is likely to be more soluble in organic solvents due to its hydrophobic benzyl substituents. Typical solvents might include dimethyl sulfoxide (DMSO) or ethanol, where non-polar characteristics can be adequately accommodated.
  • Temperature Dependence: Solubility often varies with temperature. Increased temperatures typically enhance solubility, especially for organic compounds.

In essence, the solubility of 2-benzyl-1-(benzylideneamino)guanidine will depend on several factors including polarity, the choice of solvent, and temperature. Understanding these dynamics is crucial for optimizing its use in chemical reactions and formulations.

Interesting facts

Interesting Facts about 2-benzyl-1-(benzylideneamino)guanidine

2-benzyl-1-(benzylideneamino)guanidine, a fascinating compound in the realm of organic chemistry, exhibits a variety of unique properties and applications that make it noteworthy:

  • Dual Functional Group: This compound contains both guanidine and imine functionalities, allowing for intriguing reactivity and the potential to act as a versatile intermediate in organic synthesis.
  • Biological Significance: Research has indicated that compounds like 2-benzyl-1-(benzylideneamino)guanidine can interact with various biological targets, thus showing promise for medicinal chemistry, especially in the development of new pharmaceuticals.
  • Potential Therapeutic Uses: Its structural similarities to other bioactive compounds suggest that it could be explored for use in treating conditions such as cancer or diabetes, making it a compound of interest for researchers in the fields of biochemistry and pharmacology.
  • Catalytic Properties: Certain derivatives of guanidine compounds are known to serve as effective catalysts in numerous reactions, potentially making 2-benzyl-1-(benzylideneamino)guanidine a candidate for catalytic applications in organic reactions.
  • Research Haystacks: As scientists continue to explore the myriad applications of guanidine derivatives, the detailed study of 2-benzyl-1-(benzylideneamino)guanidine may yield significant insights that bridge the gaps between organic chemistry and practical application.

In summary, 2-benzyl-1-(benzylideneamino)guanidine combines exciting chemical features with potential biological implications, making it a compound that deserves further investigation and appreciation in the scientific community. As stated by renowned chemists, "Every compound has a story; it’s our job to uncover it."