5-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate TCI A2895

Chemical Identity

CAS No.: 133464-46-7
PubChem: CID 7019067·SID 253660863
Formula: C23H23NO6
Molecular weight: 409.4 g/mol
Purity: >96.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid
SMILES: C=CCOC(=O)CC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: LRBARFFNYOKIAX-FQEVSTJZSA-N

Rp 1.326.150,00

~~Rp 942.900,00~~ Rp 1.326.150,00

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TCI A2895, also known as 5-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate, is a specialized chemical compound used in advanced laboratory research. This compound plays a crucial role in chemical and biochemical experiments, particularly in the field of peptide chemistry. Its unique structure makes it an essential component for synthesizing complex molecules and studying molecular interactions. Due to its reactivity and specificity, it is widely utilized in laboratories for precision-driven chemical reactions.

The compound is valued for its complex chemical structure, which includes an allyl group and a fluorenylmethoxy carbonyl (Fmoc) protecting group. These features contribute to its high reactivity and suitability for molecular modification. The presence of a carboxylate group further enhances its functionality in peptide synthesis and coupling reactions. Its chemical and physical properties allow it to be used in a variety of synthesis and analytical methods, making it a versatile tool for researchers.

In Indonesian laboratories, TCI A2895 is commonly used by researchers in organic chemistry, biochemistry, and pharmacology. It is frequently employed in drug development projects, molecular modification studies, and academic research. Its application spans various institutions and research centers, supporting advancements in pharmaceutical and biochemical sciences.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 19

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its Fmoc protecting group, which allows for controlled and selective coupling reactions.
Molecular Modification Studies: Its reactive functional groups enable researchers to study molecular modifications and interactions in a controlled environment.
Drug Development Research: The compound is used in the development of new pharmaceuticals, supporting the creation of complex drug molecules through chemical synthesis.
Biochemical Analysis: Its chemical properties make it suitable for biochemical assays, aiding in the study of molecular behavior and interactions.
Academic Research: It is frequently used in university and research institute laboratories for teaching and experimental purposes in chemical and biological sciences.

Brand	TCI
CAS number	133464-46-7
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	—
Physical form	—
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 sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. In laboratory settings, it is important to ensure good ventilation when working with this compound. Proper storage and handling practices help maintain its chemical integrity and ensure safe usage in research applications.

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