N-(4-aminobenzoyl)glycine
- Molecular formula
- C9H10N2O3
- CAS Number
- 2835-68-9
- IUPAC Name
- 2-[(4-aminobenzoyl)amino]acetic acid
- Molecular Weight
- 194.19g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4550g/cm3
- Synonyms
- 4-Aminohippuric acid
Identification
Interesting Facts about 2-[(4-Aminobenzoyl)amino]acetic acid
2-[(4-Aminobenzoyl)amino]acetic acid, also known as a derivative of amino acids, is a fascinating compound that showcases the versatility and complexity of organic chemistry. This compound is not just a simple structure; it serves various important functions and applications in different fields, particularly in medicinal chemistry.
Medical Significance
One of the key properties of this compound is its role in:
- Pharmaceutical Applications: It can be a potential lead compound in the development of drugs targeted at specific diseases.
- Research Programs: It is used in biochemical research to study various metabolic pathways.
Structural Highlights
The structure of 2-[(4-aminobenzoyl)amino]acetic acid includes:
- Amino groups that contribute to its reactivity and ability to form hydrogen bonds.
- Carboxylic acid functionality, making it an important candidate for proton transfer reactions.
Utility in Chemistry Education
For students and educators, this compound provides an excellent example to explore:
- Hydrogen bonding and how it influences the stability of molecules.
- Reaction mechanisms involving amines and carboxylic acids.
- Functional group transformations in organic synthesis.
As a compound rich in potential, 2-[(4-aminobenzoyl)amino]acetic acid opens avenues for innovative research and discussions in the field of chemistry. Understanding its properties not only enriches academic knowledge but also fosters curiosity towards the vast world of chemical compounds.