N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tert-leucine is a chemical compound widely used in peptide synthesis. This compound plays a crucial role in the development of complex biological molecules, particularly within the field of chemical biology. It serves as a key building block in the creation of bioactive substances and pharmaceutical compounds. Its unique chemical structure enables it to participate in various peptide coupling reactions, making it an essential component in synthetic processes.
The compound’s specific N-alkyl group contributes to its stability and reactivity, which are critical for successful peptide synthesis. Its compatibility with a wide range of chemical reagents and its ease of reaction make it a preferred choice for researchers. The high purity and solid form of the compound ensure consistent results and ease of handling in laboratory settings. These properties make it a reliable and efficient material for use in both academic and industrial research environments.
In Indonesian laboratories, this compound is commonly used in pharmacological and biochemical research. It is a vital tool for scientists working on drug development and the synthesis of bioactive compounds. Its application spans various research institutions, supporting advancements in medicinal chemistry and biological sciences. The compound’s reliability and versatility make it a standard material in many laboratory workflows.
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- Peptide Synthesis: This compound is ideal for peptide synthesis due to its reactivity and stability, allowing for the formation of complex peptide chains.
- Drug Development: It is frequently used in the development of pharmaceutical compounds, supporting the creation of bioactive molecules.
- Biochemical Research: Its role in biochemical processes makes it a valuable tool for studying molecular interactions and biological functions.
- Molecular Biology Studies: The compound is applied in molecular biology to investigate the behavior of peptides in biological systems.
- Structural Chemistry Investigations: Its unique chemical structure makes it suitable for studies focused on molecular architecture and reactivity.
| Brand | TCI |
|---|---|
| CAS number | 132684-60-7 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Chemical Biology > Peptide Chemistry |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from light |
This compound should be stored in a cool, dry environment, away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize exposure to vapors. The compound should not be exposed to incompatible substances, and all laboratory procedures should follow standard safety protocols to ensure safe handling and use.
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![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-tert-leucine (CAS 132684-60-7) - TCI F1251 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F1251.jpg?v=1769142470&width=1445)
![(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic Acid (CAS 135112-27-5) - TCI F1247 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F1247_eb046525-db9e-4cf6-88f4-4cdcf4aef85d.jpg?v=1771057940&width=533)