N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-D-alanine is a chemical compound widely used in organic and biochemical research, particularly in peptide synthesis. This compound serves as a key building block in the development of bioactive molecules, including peptides and their analogs. Its role in laboratory settings is crucial for researchers aiming to create complex molecular structures with specific functional properties. The compound is commonly employed in synthetic pathways where controlled reactivity and functional group protection are essential. Its presence in chemical biology and peptide chemistry makes it a valuable resource for advanced research projects.
The compound's unique properties, including its Boc-protected D-alanine core and the presence of a naphthyl group, make it a preferred choice for synthetic chemists. The Boc group provides stability during synthesis, allowing for selective reactions and efficient molecular modifications. The naphthyl moiety adds structural diversity and functional versatility, enabling the creation of compounds with tailored biological activities. These characteristics ensure that the compound remains stable under various reaction conditions, making it ideal for use in complex synthetic processes. Its controlled reactivity and structural integrity contribute to its widespread use in laboratory settings.
In Indonesian laboratories, this compound is frequently used in pharmaceutical research, biochemical studies, and organic material development. It plays a significant role in drug discovery programs, where the synthesis of bioactive peptides is critical. Researchers in Indonesia rely on this compound for its reliability and compatibility with various synthetic methods. Its application in academic and industrial research underscores its importance in advancing scientific knowledge and innovation in the region.
TCI brochures (PDF)
- Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 14
Related TCI products
- TCI B3617 58438-04-3 N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-L-alanine
- TCI F0882 35737-10-1 N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-beta-alanine
- TCI F0857 135673-97-1 N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-cyclohexyl-L-alanine
- TCI F0596 79990-15-1 N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-alanine
- TCI B5350 68856-96-2 N-(tert-Butoxycarbonyl)-4-methoxy-D-phenylalanine
- TCI B5322 159622-10-3 (1R,2S)-1-[(tert-Butoxycarbonyl)amino]-2-vinylcyclopropanecarboxylic Acid
- Peptide Synthesis: This compound is ideal for constructing complex peptide sequences due to its Boc-protected amino group, allowing for controlled and selective coupling reactions.
- Bioactive Compound Development: The naphthyl group contributes to the structural diversity of bioactive molecules, making it suitable for the synthesis of pharmaceutical and therapeutic agents.
- Organic Material Research: The compound's unique molecular structure supports the development of novel organic materials with specific functional properties.
- Molecular Modification Studies: Its stability and reactivity make it a valuable tool for studying molecular transformations and functional group manipulations.
- Pharmacological Research: The compound is used in drug discovery to explore the biological activity of peptides and their analogs in various therapeutic applications.
| Brand | TCI |
|---|---|
| CAS number | 76985-10-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Peptide Chemistry |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its integrity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is not flammable but should be kept away from incompatible substances. Regular monitoring of storage conditions is advised to maintain optimal performance and safety in the laboratory setting.
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Product Categories
- Chemical BiologyPeptide ChemistryAmino Acid Derivatives [Peptide Chemistry]
- Chemical BiologyPeptide ChemistryUnnatural Amino Acid Derivatives
- Pharmaceutical Development and Drug Discovery Research ReagentsPeptide ChemistryAmino Acid Derivatives [Peptide Chemistry]
- Pharmaceutical Development and Drug Discovery Research ReagentsPeptide ChemistryUnnatural Amino Acid Derivatives


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