Skip to main content

Methyl 2-[(2-amino-4-methylsulfonylphenyl)methylideneamino]-5-aminopentanoate (proposed structure based on IUPAC name)

ADVERTISEMENT
Identification
Molecular formula
C14H21N3O4S
CAS number
: Not known for this specific compound
IUPAC name
methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate
State
State

At room temperature, the compound is typically in a solid state. It is often supplied as a powder for chemical synthesis or research purposes.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
308.38g/mol
Molar mass
308.3760g/mol
Density
1.3200g/cm3
Appearence

The compound typically appears as a solid with crystalline structure. It may vary in color from white to off-white or slightly pink depending on the purity and specific formulation.

Comment on solubility

Solubility of Methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate

The solubility of methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate is influenced by several factors associated with its structural characteristics. As a compound containing both amine and sulfonamide functional groups, its solubility can be quite varied:

  • Polar Nature: Due to the presence of amino groups, which are polar, this compound is likely to exhibit increased solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents contributes to enhancing solubility in aqueous environments.
  • Molecular Size: Larger molecular structures might hinder solubility to some extent, making it necessary to consider molecular weight when predicting solubility behavior.
  • pH Dependency: The ionization of the amine groups can be influenced by the pH of the solution, affecting overall solubility; thus, it may appear more soluble in acidic or basic conditions.

In summary, the solubility behavior of methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate could be described as multifaceted, dependent on factors such as polarity, hydrogen bonding capacity, and environmental pH levels. Understanding these dynamics is essential for practical applications involving this compound.

Interesting facts

Methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate

This compound is a fascinating example of a complex organic molecule, often of interest in the fields of medicinal chemistry and drug design. Methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate serves as a potential building block for various bioactive compounds due to its unique structure.

Interesting Facts:

  • Structural Complexity: The presence of multiple functional groups, including sulfonamides and amino acids, showcases the compound's potential for creating derivatives with tailored properties.
  • Biological Relevance: Compounds similar to this one can play critical roles in enzyme inhibition, making them valuable in studying metabolic pathways.
  • Research Applications: Methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate may be employed in various research studies aimed at synthesizing new pharmaceuticals, particularly those that target specific receptors in the body.
  • Synthetic Pathways: The synthesis of this compound can be achieved through several methods, often involving multi-step reactions that highlight the versatility of organic synthesis techniques.
  • Potential Therapeutic Uses: Given its structural attributes, this compound could influence pathways related to inflammation, cancer, and other diseases, warranting further investigation.

In summary, the compound methyl 2-amino-5-[[amino-(p-tolylsulfonylamino)methylene]amino]pentanoate represents the intersection of structural complexity and biological significance, making it a compelling subject for further research in chemical sciences.

Synonyms
SCHEMBL4452449
DTXSID101009157
Methyl N~5~-[N-(4-methylbenzene-1-sulfonyl)carbamimidoyl]ornithinate