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2-(N-benzylanilino)-N'-hydroxy-acetamidine

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Identification
Molecular formula
C15H17N3O
CAS number
. CAS number not available
IUPAC name
2-(N-benzylanilino)-N'-hydroxy-acetamidine
State
State

At room temperature, 2-(N-benzylanilino)-N'-hydroxy-acetamidine is generally found in a solid state, reflecting its crystalline nature. The solid form is stable under standard conditions of temperature and pressure.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
288.50
Boiling point (Kelvin)
561.70
General information
Molecular weight
238.32g/mol
Molar mass
238.2900g/mol
Density
1.2030g/cm3
Appearence

The compound 2-(N-benzylanilino)-N'-hydroxy-acetamidine typically appears as a solid with crystalline texture. The color can vary depending on the purity and specific form, but it is often a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(N-benzylanilino)-N'-hydroxy-acetamidine

2-(N-benzylanilino)-N'-hydroxy-acetamidine is a compound that exhibits interesting solubility characteristics, influenced by its structure and functional groups. Understanding the solubility of this compound is essential for various applications, including pharmaceuticals and research.

Factors Influencing Solubility

  • Polarity: The presence of the hydroxy (-OH) group enhances the compound's ability to interact with polar solvents, such as water.
  • Hydrogen Bonding: The capacity for hydrogen bonding due to the -OH and amine groups can lead to increased solubility in polar solvents.
  • Size and Structure: The large benzyl and aniline moieties may decrease solubility in very polar solvents due to steric hindrance and increased hydrophobic character.

Generally, we can outline the expected solubility behavior as follows:

  • Highly soluble in: polar solvents, especially alcohols and potentially aqueous solutions, due to hydrogen bonding.
  • Moderately soluble in: less polar solvents, depending on the steric factors imposed by the benzyl and anilino groups.
  • Limited solubility in: non-polar solvents, where the hydrophobic regions dominate solute-solvent interactions.

In conclusion, the solubility of 2-(N-benzylanilino)-N'-hydroxy-acetamidine is dictated by a balance of polar interactions and steric effects, making it suitable for various applications where solubility in polar environments is advantageous. Understanding these properties can significantly aid in predicting its behavior in chemical reactions and formulations.

Interesting facts

Interesting Facts about 2-(N-benzylanilino)-N'-hydroxy-acetamidine

2-(N-benzylanilino)-N'-hydroxy-acetamidine, a fascinating compound, has garnered the attention of chemists due to its unique structure and potential applications. Here are some engaging insights about this compound:

  • Structure and Functionality: The compound possesses a complex structure characterized by the presence of a hydroxylamine group, which enhances its reactivity. This structure enables the compound to participate in various chemical reactions, making it versatile in synthetic pathways.
  • Biological Relevance: Compounds similar to this one have been investigated for their biological activities, particularly as potential pharmaceuticals. They might exhibit properties such as anti-cancer and anti-inflammatory effects, which is crucial for drug discovery.
  • Research Applications: The compound is of interest in materials science and organic synthesis due to its ability to form hydrogen bonds. This quality makes it a candidate for developing new materials with desired thermal and mechanical properties.
  • Historical Context: Hydroxy-acetamidine derivatives have been part of research for many years, often used to create more complex organic compounds that could lead to breakthroughs in both medicinal and material chemistry.

“Understanding complex compounds like 2-(N-benzylanilino)-N'-hydroxy-acetamidine can lead to innovative solutions and advancements in various scientific fields.”

In summary, 2-(N-benzylanilino)-N'-hydroxy-acetamidine stands out for its intriguing chemical properties and potential applications that span across various domains within chemistry. Its ongoing study promises to reveal more about its utility and effects, fostering advancements in scientific research.

Synonyms
25394-78-9
SCHEMBL138303
DTXSID30944862
CID 31044