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2,4-bis(benzylamino)-4-oxobutanoic acid

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Identification
Molecular formula
C18H20N2O3
CAS number
Not Available
IUPAC name
2,4-bis(benzylamino)-4-oxo-butanoic acid
State
State

At room temperature, 2,4-bis(benzylamino)-4-oxobutanoic acid is in a solid state. The material is relatively stable when stored in a dry, cool environment, protected from moisture and intense light.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
312.38g/mol
Molar mass
312.3800g/mol
Density
1.2400g/cm3
Appearence

2,4-bis(benzylamino)-4-oxobutanoic acid appears as a crystalline solid. The crystals are often off-white to pale yellow in color, indicating its purity, and may have a slightly shiny or lustrous surface depending on the method of crystallization.

Comment on solubility

Solubility of 2,4-bis(benzylamino)-4-oxo-butanoic acid

The solubility of 2,4-bis(benzylamino)-4-oxo-butanoic acid can be influenced by several factors, making it a topic of interest in both theoretical and practical applications. This compound contains both hydrophilic and hydrophobic groups, which play a significant role in its overall solubility characteristics.

Factors Affecting Solubility

  • Polarity: The presence of amino groups enhances its ability to interact with water, potentially increasing solubility in polar solvents.
  • Hydrogen Bonding: The carboxylic acid group can form hydrogen bonds, which can facilitate solubility in polar environments.
  • Hydrophobic Interactions: The benzyl groups introduce hydrophobic character; thus, solubility may decrease in purely aqueous solutions.
  • Temperature: Solubility is generally temperature-dependent; higher temperatures may increase solubility for many organic compounds.

In summary, while 2,4-bis(benzylamino)-4-oxo-butanoic acid has the potential for good solubility in polar solvents due to its functional groups, its overall solubility profile may vary based on environmental conditions. As with many organic compounds, a balance of interactions is key—"it's not just about what you have, but how you use it!"

Interesting facts

Interesting Facts about 2,4-bis(benzylamino)-4-oxo-butanoic acid

This unique compound, 2,4-bis(benzylamino)-4-oxo-butanoic acid, has garnered attention in various fields of research, particularly in medicinal chemistry. Here are some fascinating aspects that highlight its significance:

  • Amino Acids Connection: This compound features amino groups that can be crucial for interactions in biological systems, particularly in the design of pharmaceuticals.
  • Potential Therapeutic Applications: Research suggests that compounds with similar structures can exhibit antimicrobial and anti-inflammatory properties, opening up possibilities for new drug formulations.
  • Innovative Synthesis: The method of synthesizing this compound can inspire various synthetic routes in organic chemistry. The incorporation of benzylamine groups may allow for unique functionalizations.
  • Structure-Activity Relationship (SAR): The presence of both benzyl groups and a keto functionality can provide insights into SAR studies, helping chemists understand the mechanisms behind biological activity.
  • Contemporary Relevance: As researchers continually explore the synthesis and application of complex molecules, compounds like 2,4-bis(benzylamino)-4-oxo-butanoic acid may play a role in the development of innovative materials and drugs.

In summary, the exploration of 2,4-bis(benzylamino)-4-oxo-butanoic acid not only enhances our understanding of chemical interactions but also inspires future research in drug development and synthetic methodologies. As the field progresses, such compounds remind us of the endless possibilities within the realm of chemistry.

Synonyms
25800-55-9
ASPARAGINE, N,N(sup 2)-DIBENZYL-, DL-
RefChem:1077301
DL-N,N(sup 2)-Dibenzylasparagine
2-(BENZYLAMINO)-3-(BENZYLCARBAMOYL)PROPANOIC ACID
BRN 2668305
N,N~2~-dibenzylasparagine
4-12-00-02348 (Beilstein Handbook Reference)
DTXSID30948704
N-Benzyl-4-(benzylimino)homoserine
STL228867
AKOS002229298
AKOS016165088
AZ-6012
ST45177920
2-[benzylamino]-3-[N-benzylcarbamoyl]propanoic acid