N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-L-alanine TCI B3617

Chemical Identity

CAS No.: 58438-04-3
PubChem: CID 7020908·SID 125307515
Formula: C18H21NO4
Molecular weight: 315.4 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-naphthalen-2-ylpropanoic acid
SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CC2=CC=CC=C2C=C1)C(=O)O
InChIKey: URKWHOVNPHQQTM-HNNXBMFYSA-N

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N-(tert-Butoxycarbonyl)-3-(2-naphthyl)-L-alanine is a chemical compound widely used in organic and biochemical research, particularly in peptide synthesis. This compound plays a crucial role in laboratory settings where controlled chemical reactions and selective functional group manipulation are required. Its complex structure enables it to serve as a building block for the creation of biologically active molecules. In the field of chemical biology, it is essential for the development of peptides and their analogs, which are vital for drug discovery and biotechnology applications.

The compound’s unique properties make it a preferred choice for researchers. It contains a tert-butoxycarbonyl (Boc) group, which acts as a protecting group for the amino function. This allows for precise control over chemical reactions, ensuring that only the desired parts of the molecule undergo modification. Its stability under certain conditions, combined with its reactivity in controlled environments, makes it ideal for use in synthetic processes requiring high selectivity. The Boc group can be selectively removed under specific conditions, enabling the synthesis of more complex molecules with high efficiency.

In Indonesian laboratories, this compound is commonly used in organic and biochemical research. It is frequently found in projects related to the synthesis of bioactive compounds, especially in academic and research institutions. Its role in peptide chemistry makes it a valuable resource for scientists working on drug development and biotechnology applications. Its application is widespread in both educational and industrial research settings, supporting the advancement of chemical and biological sciences.

TCI brochures (PDF)

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

Related TCI products

Peptide Synthesis: This compound is ideal for synthesizing peptides due to its Boc protecting group, which allows controlled amino acid coupling reactions.
Drug Discovery Research: It is used in the development of bioactive peptides and analogs, supporting pharmaceutical research and innovation.
Organic Chemistry Studies: Its complex structure makes it a key reagent in organic synthesis, enabling the creation of diverse molecular structures.
Biochemical Analysis: It is employed in biochemical experiments to study molecular interactions and functional group behavior.
Biotechnology Applications: It supports the production of biologically active compounds, aiding in the development of new therapeutic agents.

Brand	TCI
CAS number	58438-04-3
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid powder
Storage	Store in a dry, cool, and dark place away from moisture and air exposure

This compound should be stored in a dry, cool, and dark environment to prevent degradation due to moisture and air exposure. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its chemical stability. Due to its sensitivity to humidity, it is important to ensure that the storage area is well-controlled and free from contaminants. In laboratory settings, it should be handled with care using appropriate personal protective equipment to avoid direct contact. Regular monitoring of storage conditions is essential to maintain the integrity and effectiveness of the compound in research applications.

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