D-Phenylalanine
- Molecular formula
- C9H11NO2
- CAS Number
- 673-06-3
- IUPAC Name
- 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid
- Molecular Weight
- 165.19g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3500g/cm3
- Synonyms
- alpha-Methyl-m-tyrosine
Identification
Interesting Facts about 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid
2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid, often referred to as a derivative of the well-known amino acid, is fascinating for several reasons:
- Role in Biochemistry: This compound plays a crucial role in various biochemical processes, particularly in metabolism and protein synthesis.
- Potential Medicinal Uses: Due to its structural similarity to amino acids, it may exhibit properties that can be exploited for therapeutic applications, such as in the treatment of neurological disorders.
- Phenolic Connection: The presence of the hydroxyphenyl group introduces unique electron-donating properties, which can affect the compound's reactivity and interactions with biological systems.
- Steric Hindrance: The methyl group attached to the central carbon increases steric hindrance, affecting how this compound interacts with enzymes and receptors, which is a critical aspect in drug design.
- Research Significance: Ongoing research into this compound may unveil new insights into amino acid derivatives and their implications in fields such as medicinal chemistry, pharmacology, and nutrition.
As you delve into the study of this compound, keep in mind the intricacies of its structure and the myriad of ways it can influence biological systems. In the words of a famous chemist, "Chemistry is the central science" - bridging gaps and opening doors to understanding life's processes.
Whether you are a chemistry student or a seasoned researcher, exploring compounds like 2-amino-3-(3-hydroxyphenyl)-2-methyl-propanoic acid will deepen your appreciation for the complexity and beauty of chemical interactions!