Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric Acid: A Key Chiral Building Block
In the realm of chemical synthesis, particularly in pharmaceutical and fine chemical industries, chiral building blocks are indispensable. Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid, identified by its CAS number 268734-29-8, is a prime example of such a valuable chiral intermediate. Its specific stereochemistry and functional groups make it a sought-after component for creating enantiomerically pure compounds, essential for drug efficacy and safety.
The term 'chiral' refers to molecules that are non-superimposable on their mirror images, much like left and right hands. In drug development, a specific enantiomer often exhibits the desired therapeutic activity, while the other may be inactive or even cause adverse effects. Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid, with its designated (R) configuration, provides researchers with a means to incorporate this specific chirality into target molecules. The Fmoc protecting group facilitates its use in sequential synthesis methods, while the 2-chlorophenyl moiety can impart unique electronic and steric properties, influencing molecular interactions.
For procurement professionals and research scientists, the ability to buy Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid from a reputable manufacturer is crucial. When exploring options, consider keywords such as 'Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid supplier China' to identify experienced suppliers. Companies like NINGBO INNO PHARMCHEM CO.,LTD. are dedicated to supplying high-quality chiral intermediates, understanding the stringent requirements of the pharmaceutical sector. Obtaining a price quote from such manufacturers ensures you are investing in product integrity and a reliable supply chain.
The application of this chiral building block extends beyond peptide synthesis into the broader field of medicinal chemistry and organic synthesis. Its incorporation can lead to novel compounds with improved pharmacological profiles. Therefore, securing a consistent and high-purity source for Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid is a strategic move for any organization involved in the development of advanced chemicals and pharmaceuticals. Always prioritize suppliers who can provide detailed specifications and consistent product quality.
Perspectives & Insights
Molecule Vision 7
“In drug development, a specific enantiomer often exhibits the desired therapeutic activity, while the other may be inactive or even cause adverse effects.”
Alpha Origin 24
“Fmoc-(R)-3-Amino-4-(2-chlorophenyl)butyric acid, with its designated (R) configuration, provides researchers with a means to incorporate this specific chirality into target molecules.”
Future Analyst X
“The Fmoc protecting group facilitates its use in sequential synthesis methods, while the 2-chlorophenyl moiety can impart unique electronic and steric properties, influencing molecular interactions.”