N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-norvaline TCI F1117

Chemical Identity

Other names: N-Fmoc-L-norvaline · Fmoc-Nva-OH
CAS No.: 135112-28-6
Formula: C20H21NO4
Molecular weight: 339.39 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid
SMILES: CCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: JBIJSEUVWWLFGV-SFHVURJKSA-N
MDL: MDL00155631
PubChem: CID 7016885

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-norvaline is a chemical compound widely used in peptide chemistry and organic synthesis. It serves as a key building block in the development of complex molecules, particularly in biochemical and pharmacological research. This compound is essential for creating high-reactivity molecules that are integral to advanced chemical synthesis processes. Its unique structure enables it to participate in selective chemical reactions, making it a valuable tool for researchers aiming to achieve precise molecular modifications.

The compound's structure, featuring a fluoren-9-ylmethoxy carbonyl group, provides it with specific reactivity and selectivity. These properties make it a preferred choice for synthesizing peptides and other bioactive compounds. Its stability under certain conditions, combined with its reactivity in substitution and bond-forming reactions, ensures its utility in various synthetic pathways. The ability to selectively bind with other amino acids enhances its role in creating complex molecular structures with high precision.

In Indonesian laboratories, this compound is commonly used in applied research such as drug development, molecular interaction studies, and the synthesis of bioactive compounds. Due to its complex structure and high reactivity, it is frequently employed in laboratories focused on advanced chemical and biological research. Its versatility and reliability make it an essential component in the toolkit of chemists and biochemists working on innovative projects.

Drug development research benefits from this compound's ability to participate in selective chemical reactions, enabling the synthesis of complex pharmaceutical compounds with high precision.
Molecular interaction studies utilize its unique structure to investigate how it interacts with other amino acids, aiding in the understanding of biochemical processes.
Peptide synthesis applications rely on its reactivity and selectivity, allowing for the creation of customized peptide sequences with specific functional properties.
Bioactive compound synthesis leverages its stability and reactivity to produce molecules with therapeutic potential in pharmaceutical and biotechnology fields.
Advanced chemical synthesis projects use its structural versatility to design and create novel compounds with tailored chemical properties for various scientific applications.

Brand	TCI
CAS number	135112-28-6
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its reactivity. Proper labeling of containers is essential for safe handling and identification. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Ensuring that storage conditions are controlled helps preserve its effectiveness for use in research applications.

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