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Description
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-2-phenylglycine is a chemical compound widely used in laboratory settings, particularly in peptide chemistry. It serves as a protecting group in peptide synthesis, helping to control and direct chemical reactions by temporarily blocking reactive sites. This compound plays a crucial role in ensuring the accuracy and efficiency of synthetic processes, especially when constructing complex molecular structures. Its application extends to various fields such as pharmaceutical research and biochemical studies, where precise molecular manipulation is essential.
The compound is valued for its chemical stability and specificity. It reacts selectively with various reagents, making it a reliable choice for controlled chemical transformations. Its molecular structure allows it to form stable bonds with amino acid groups, facilitating the assembly of peptide chains with high fidelity. These properties make it a preferred reagent in synthetic chemistry, where consistency and predictability are key. Its ability to resist unwanted side reactions further enhances its utility in laboratory environments.
In Indonesian laboratories, this compound is commonly used in organic and biochemical research. It is an essential tool for researchers working on drug development and molecular biology projects. Its availability in the local market supports scientific innovation by providing access to high-quality reagents. Researchers in universities and research institutions rely on it to advance their studies in peptide synthesis and related disciplines. Its role in enabling precise chemical reactions underscores its importance in modern laboratory practices.
Laboratory Applications
Peptide Synthesis: This compound is ideal for constructing complex peptide structures due to its ability to act as a protecting group, preventing unwanted side reactions during synthesis.
Pharmaceutical Research: It supports the development of new drugs by enabling the controlled synthesis of bioactive peptides, which are critical in drug discovery.
Biochemical Studies: Its use in biochemical experiments allows for the precise modification of amino acid sequences, aiding in the study of protein structures and functions.
Organic Chemistry Research: It is a preferred reagent in organic synthesis due to its stability and reactivity, making it suitable for a wide range of chemical transformations.
Molecular Biology Applications: It facilitates the synthesis of peptides used in molecular biology, such as those involved in enzyme studies and receptor interactions.
Specifications
Brand: TCI
CAS number: 102410-65-1
Category: Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes: Available in various quantities as per supplier specifications
Physical form: Solid powder
Storage note: Store in a cool, dry place away from moisture and light
Handling and Storage
This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that storage conditions are consistent to avoid degradation. Avoid direct sunlight and high humidity, as these can affect its integrity. Proper labeling of containers is essential for safe handling and to prevent accidental use. Always follow standard laboratory safety protocols when working with this compound.
![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-2-phenylglycine (CAS 102410-65-1) - TCI F0669 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F0669.jpg?v=1771058185&width=1946)
![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-2-phenylglycine (CAS 102410-65-1) - TCI F0669 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F0669.jpg?v=1771058185&width=1445)
