Z-His-OH: A Versatile Building Block for Chemical Synthesis
While Z-His-OH (CAS: 14997-58-1) is most prominently recognized for its indispensable role in peptide synthesis, its utility as a versatile chemical building block extends into broader applications within organic chemistry and fine chemical manufacturing. This protected amino acid derivative, N-alpha-Carbobenzyloxy-L-histidine, offers a unique combination of functionalities that make it valuable for creating a diverse array of complex organic molecules.
The core structure of Z-His-OH features the L-histidine amino acid, characterized by its imidazole ring side chain. This imidazole moiety is a nitrogen-containing heterocycle that can participate in a variety of chemical reactions, including nucleophilic substitutions, electrophilic attacks, and coordination with metal ions. Coupled with the alpha-amino group protected by the carbobenzyloxy (Z) group and the carboxyl group, Z-His-OH presents multiple points for chemical modification and elaboration.
In organic synthesis, chemists often seek starting materials that can introduce specific functional groups or heterocyclic systems into target molecules. Z-His-OH fulfills this role effectively. For instance, the imidazole ring can be derivatized, alkylated, or used in coupling reactions to form new carbon-carbon or carbon-heteroatom bonds. The protected carboxyl group can be activated for esterification or amidation, further expanding the synthetic possibilities. Researchers often look to buy Z-His-OH when designing synthetic routes for biologically active compounds, pharmaceuticals, or advanced materials.
Beyond its application in peptide bond formation, Z-His-OH can be employed in the synthesis of:
- Medicinal Chemistry Intermediates: Its structure can be incorporated into scaffolds for new drug candidates, especially those targeting pathways where histidine's chemical properties are crucial, such as metalloenzymes.
- Ligands for Catalysis: The imidazole ring's ability to coordinate with metal ions makes Z-His-OH and its derivatives potential ligands for homogeneous catalysis.
- Functional Materials: The unique properties of the imidazole ring could be exploited in the development of specialized polymers or surface modification agents.
For chemical manufacturers and procurement specialists, sourcing Z-His-OH requires attention to purity and consistency. A reliable Z-His-OH manufacturer or supplier is key to ensuring that the material meets the stringent requirements for complex organic synthesis. While searching for the best Z-His-OH price, it is important to consider the overall value, including product quality, availability, and the supplier's technical support. Companies looking to secure a consistent supply of CAS 14997-58-1 for their fine chemical production should prioritize partnerships with established chemical suppliers.
In conclusion, the versatility of Z-His-OH as a chemical building block should not be underestimated. Its reactive functionalities and inherent structural features make it a valuable asset for synthetic chemists aiming to construct intricate organic molecules for a wide range of applications, from pharmaceuticals to advanced materials. A dependable supply from a qualified Z-His-OH supplier empowers innovation in chemical synthesis.
Perspectives & Insights
Future Origin 2025
“This imidazole moiety is a nitrogen-containing heterocycle that can participate in a variety of chemical reactions, including nucleophilic substitutions, electrophilic attacks, and coordination with metal ions.”
Core Analyst 01
“Coupled with the alpha-amino group protected by the carbobenzyloxy (Z) group and the carboxyl group, Z-His-OH presents multiple points for chemical modification and elaboration.”
Silicon Seeker One
“In organic synthesis, chemists often seek starting materials that can introduce specific functional groups or heterocyclic systems into target molecules.”