N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-phenylalanine TCI F1167

Chemical Identity

Other names: N-Fmoc-N-methyl-L-phenylalanine · Fmoc-N-Me-Phe-OH
CAS No.: 77128-73-5
PubChem: CID 978356·SID 354334545
Formula: C25H23NO4
Molecular weight: 401.46 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-phenylpropanoic acid
SMILES: CN(C(CC1=CC=CC=C1)C(=O)O)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
InChIKey: GBROUWPNYVBLFO-QHCPKHFHSA-N
MDL: MDL00151938

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-phenylalanine is a chemical compound widely used in chemical and biochemical experiments, particularly in peptide synthesis. This compound plays a crucial role in laboratory settings where precise chemical reactions are required. Its complex structure allows it to act as a building block in the formation of peptide chains through peptidization reactions. It is commonly used in organic chemistry and biochemistry to create molecules with specific biological activities.

The compound is valued for its chemical stability and its ability to participate in various reactions such as esterification and hydrolysis. Its specific molecular structure enables high precision in chemical reactions, making it an ideal choice for research that demands controlled and reproducible outcomes. This property is especially important in applications where the accuracy of chemical interactions is critical. Its reliability and versatility have made it a preferred material in both academic and industrial research environments.

In Indonesian laboratories, this compound is frequently used in biochemical and pharmacological research. Scientists in educational and research institutions rely on it to develop new compounds with potential therapeutic applications. It is also integral to experiments in organic chemistry and peptide synthesis, contributing to advancements in drug discovery and molecular biology. Its application spans multiple scientific disciplines, reinforcing its importance in modern laboratory practices.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 22

Related TCI products

Peptide Synthesis: This compound is ideal for synthesizing peptides due to its ability to form stable peptide bonds through peptidization reactions.
Biochemical Research: Its chemical stability and reactivity make it suitable for experiments involving enzyme interactions and protein modifications.
Organic Chemistry Experiments: It is commonly used in the synthesis of organic compounds with specific functional groups and biological activities.
Drug Discovery: Researchers use it to develop new therapeutic agents by modifying its structure to enhance biological activity.
Molecular Biology Studies: Its role in controlled chemical reactions supports studies on molecular interactions and structural modifications.

Brand	TCI
CAS number	77128-73-5
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 light

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. Due to its chemical stability, it does not require refrigeration but should be protected from potential contaminants. In laboratory settings, it is important to handle it with appropriate personal protective equipment to ensure safety. Proper labeling and storage conditions help maintain its integrity and effectiveness in experimental applications. Always ensure that the storage area is well-ventilated and free from incompatible substances to prevent any chemical interactions.

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