N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-leucine TCI F0295

Chemical Identity

Other names: N-Fmoc-L-leucine · Fmoc-Leu-OH
CAS No.: 35661-60-0
Formula: C21H23NO4
Molecular weight: 353.42 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylpentanoic acid
SMILES: CC(C)CC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: CBPJQFCAFFNICX-IBGZPJMESA-N
MDL: MDL00037133
PubChem: CID 1549133

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-leucine is a chemical compound widely used in peptide synthesis and biochemical research. This compound plays a crucial role in the coupling of amino acids to form peptide chains, making it an essential reagent in organic chemistry and biochemistry laboratories. Its structural complexity and reactivity make it a versatile tool for creating complex molecules with specific biological activities. It is commonly used as a building block in the development of bioactive compounds, including pharmaceuticals and biotechnology products.

The compound's stability and reactivity under controlled conditions make it a preferred choice for researchers. It dissolves well in organic solvents such as acetone and ethyl acetate, facilitating its use in various chemical reactions. Its ability to undergo specific reactions, such as hydrolysis and conjugation with other molecules, enhances its applicability in diverse experimental setups. These properties ensure that it remains a reliable and efficient reagent in both academic and industrial research environments.

In Indonesian laboratories, this compound is frequently used in biochemical, pharmacological, and materials science research. It supports the development of new drugs, the study of protein structures, and the creation of advanced materials. Its high purity and consistent performance make it a trusted component in the work of researchers and scientists across various disciplines.

Peptide Synthesis: This compound is ideal for synthesizing peptides due to its ability to form stable amide bonds during coupling reactions.
Biochemical Research: It is used in studies involving amino acid interactions and molecular binding due to its structural compatibility with biological systems.
Drug Development: Its role in creating bioactive molecules makes it valuable in pharmaceutical research and compound screening.
Organic Chemistry Experiments: The compound's solubility and reactivity make it suitable for a wide range of synthetic reactions in organic chemistry.
Material Science Studies: It is used in the development of functional materials that require specific molecular interactions and chemical stability.

Brand	TCI
CAS number	35661-60-0
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. It is important to keep the compound away from incompatible substances and to follow standard laboratory protocols for chemical storage and disposal. Proper labeling and storage conditions are essential to maintain its effectiveness and ensure safe handling in research environments.

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