Interesting facts
Interesting Facts about 2-(Benzylamino)butanedioic Acid
2-(Benzylamino)butanedioic acid is a fascinating compound that captures the interest of many chemists due to its unique structure and potential applications. Here are some intriguing insights about this compound:
- Structure and Functionality: The compound features a butanedioic acid framework with a benzylamino group attached, making it a valuable building block in organic synthesis. Its dual functionality allows for a variety of chemical reactions and modifications, which can be harnessed for diverse applications.
- Chirality: The presence of the chiral center in the butanedioic backbone provides opportunities for the study of stereochemistry and its implications in biological systems. Chirality plays a critical role in the function of many biomolecules, and compounds like this one can be investigated for their enantiomeric effects.
- Potential Biological Activity: Certain analogs of butanedioic acids exhibit bioactivity. Researchers are exploring the potential health benefits of this compound in medical chemistry, especially in drug design and development. Its derivatives may possess interesting pharmacological properties.
- Applications in Material Science: The compound's structural features lend themselves to applications in polymers and materials science. The ability to incorporate it into larger polymer chains could lead to materials with enhanced properties, such as improved strength or functionality.
- Research Utility: 2-(Benzylamino)butanedioic acid serves as an important intermediate in the synthesis of various compounds. Its ability to act as a ligand in coordination chemistry also opens up potential for use in catalysis and materials development.
In summary, 2-(benzylamino)butanedioic acid is a versatile compound with a range of intriguing properties. Whether in organic synthesis, drug development, or materials science, its unique features pave the way for exciting research opportunities.
Synonyms
5555-22-6
N-Benzyl-DL-aspartic acid
N-benzyl aspartic acid
2-(benzylamino)butanedioic acid
N-benzylaspartic acid
Benzylaspartic acid
ASPARTIC ACID, N-BENZYL-, DL-
iem-1770
2BV23TSD8J
aspartic acid, N-(phenylmethyl)-
NSC-60241
DL-N-Benzylaspartic acid
EINECS 226-917-8
NSC 60241
UNII-2BV23TSD8J
(2R)-2-(benzylamino)butanedioic acid
MFCD00020501
NSC163081
SCHEMBL60483
2-(Benzylamino)succinic acid
N-(Phenylmethyl)aspartic acid
butanedioic acid, benzylamino-
RKSKSWSMXZYPFW-UHFFFAOYSA-N
DTXSID601307665
ALBB-025620
NSC60241
DL-Aspartic acid, N-(phenylmethyl)-
AKOS004912628
NSC-163081
N-BenZylaspartic acid (BZl-DL-Asp-OH)
LS-08653
CS-0319832
H35226
Q27254535
91199-26-7
Solubility of 2-(benzylamino)butanedioic acid
The solubility of 2-(benzylamino)butanedioic acid is an interesting topic, as it exhibits unique characteristics due to its chemical structure. This compound is a derivative of amino acids, which influences its solubility in various solvents.
Typically, its solubility can be described in the following ways:
In practical applications, understanding the solubility of 2-(benzylamino)butanedioic acid is crucial for pharmaceutical formulations, as it can greatly affect the compound's bioavailability and therapeutic effectiveness. As a summary, one could state that:
Thus, careful consideration of the solvent environment is necessary when working with 2-(benzylamino)butanedioic acid.