N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-trans-(tert-butoxy)-L-proline TCI F1095

Chemical Identity

Other names: N-Fmoc-4-trans-(tert-butoxy)-L-proline · Fmoc-Hyp(tBu)-OH
CAS No.: 122996-47-8
PubChem: CID 978347·SID 354334435
Formula: C24H27NO5
Molecular weight: 409.48 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S,4R)-1-(9H-fluoren-9-ylmethoxycarbonyl)-4-[(2-methylpropan-2-yl)oxy]pyrrolidine-2-carboxylic acid
SMILES: CC(C)(C)OC1CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O
InChIKey: WPBXBYOKQUEIDW-VFNWGFHPSA-N
MDL: MDL00151930

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-trans-(tert-butoxy)-L-proline is a chemical compound widely used in peptide synthesis. This compound plays a critical role in chemical biology, particularly in the field of peptide chemistry. It is commonly employed in laboratory settings to facilitate the controlled formation of peptide bonds and the modification of amino acid chains. Its unique structure allows for precise chemical reactions, making it an essential tool for researchers working on complex molecular structures.

The compound’s high reactivity and specific functional groups, such as the tert-butoxycarbonyl (Boc) group, make it a preferred choice in synthetic processes. The Boc group acts as a protecting group for the amino function, enabling selective chemical reactions and preventing unwanted side reactions. This property ensures greater control and efficiency in peptide synthesis, which is crucial for developing bioactive compounds. Its stability under specific reaction conditions further enhances its utility in laboratory environments.

In Indonesian laboratories, this compound is frequently used in organic chemistry, biochemical research, and pharmacological studies. It supports the development of new drugs and the analysis of biomolecules. Researchers in universities and research institutions rely on this compound for molecular interaction studies and the synthesis of complex peptides. Its versatility and reliability make it a standard component in many laboratory workflows.

Related TCI products

Peptide Synthesis: This compound is ideal for constructing peptide chains due to its ability to form stable peptide bonds under controlled conditions.
Amino Acid Modification: Its Boc protecting group allows for precise modification of amino acid sequences, enhancing the accuracy of biochemical experiments.
Drug Development: It supports the synthesis of bioactive compounds, aiding in the creation of new pharmaceuticals and therapeutic agents.
Biomolecular Analysis: The compound is used in the study of molecular interactions, providing insights into biological processes and molecular behavior.
Organic Chemistry Research: Its reactivity and structural complexity make it a valuable tool for exploring chemical reactions and synthetic pathways.

Brand	TCI
CAS number	122996-47-8
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 moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid exposure to direct sunlight and ensure proper ventilation in the workspace. The compound is not flammable, but it should be stored separately from incompatible materials to prevent any potential chemical interactions. Regular inspection of storage conditions is advised to ensure long-term stability and usability in laboratory applications.

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