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Benzamidine

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Identification
Molecular formula
C15H16N4
CAS number
1670-14-0
IUPAC name
1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine
State
State

Benzamidine is generally encountered in its hydrochloride salt form, which is typically solid at room temperature.

Melting point (Celsius)
229.00
Melting point (Kelvin)
502.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
211.32g/mol
Molar mass
211.2650g/mol
Density
1.0990g/cm3
Appearence

Benzamidine hydrochloride is typically a white crystalline powder.

Comment on solubility

Solubility of 1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine

1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine is a compound that exhibits unique solubility characteristics. This guanidine derivative is generally soluble in polar solvents, which can influence its application in various chemical environments. Key points regarding its solubility are as follows:

  • Polar Solvents: The compound shows good solubility in substances such as water and alcohols due to its polar functional groups.
  • Non-Polar Solvents: In contrast, it has limited solubility in non-polar solvents. This is typical for many compounds containing amino groups, which favor interactions with polar environments.
  • Temperature Dependence: Solubility can increase with temperature; as with many organic compounds, heating can promote the dissolution process.

In practical applications, it is crucial to consider solubility when formulating solutions for biological or chemical analyses. As stated in various literature, "the solubility profile is paramount for understanding the behavior of compounds in solution." Thus, for chemists working with this guanidine, selecting the right solvent can significantly impact the compound's efficacy and usability.

Interesting facts

Interesting Facts about 1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine

1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine is a fascinating compound that showcases the versatility of guanidine derivatives in various fields of chemistry. Here are some captivating aspects:

  • Biological Activity: This compound is notable for its potential biological applications, particularly in the development of pharmacological agents. Guanidine derivatives often exhibit antimicrobial and antineoplastic properties, making this compound a potential candidate for drug discovery.
  • Structural Features: The structure of 1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine includes a guanidine core which is enhanced by a benzyl and phenyl group. This combination can influence its reactivity and biological activity significantly.
  • Research Applications: Researchers are continually exploring the properties of guanidine derivatives in areas such as catalysis, material science, and medicinal chemistry. The unique structure of this compound may lead to innovative applications.
  • Mechanism of Action: Many guanidine derivatives operate by interacting with various biological targets, including enzymes and receptors. Understanding the precise mechanism of action of this compound could lead to the development of targeted therapies.

In essence, 1-benzyl-3-(diaminomethylene)-1-phenyl-guanidine is more than just a chemical entity; it's a key to unlocking potential advancements in pharmaceuticals and biochemistry. As we delve deeper into its properties, we may uncover new pathways for creating effective therapeutic agents.

Synonyms
CHEMBL5315359
SCHEMBL28129340
N-benzyl-N-phenyldicarbonimido/ic diamide/imido
AH-034/33507020