N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine TCI F0454

Chemical Identity

Other names: N-Fmoc-L-serine · Fmoc-Ser-OH
CAS No.: 73724-45-5
Formula: C18H17NO5
Molecular weight: 327.34 g/mol
Purity: >97.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid
SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CO)C(=O)O
InChIKey: JZTKZVJMSCONAK-INIZCTEOSA-N
MDL: MDL04113634
PubChem: CID 6541433

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine is a chemical compound widely used in peptide chemistry and organic synthesis. This compound plays a crucial role in laboratory settings where precise functional group manipulation is required. It is commonly employed in the synthesis of peptides and the modification of complex molecules, making it an essential reagent in chemical biology research. Its unique structure allows for controlled reactions under specific conditions, enhancing the accuracy of experimental outcomes.

The compound's high purity and stable molecular structure make it a preferred choice for researchers seeking reliable and reproducible results. The fluoren-9-ylmethoxy group acts as a protective group for the carboxylate, ensuring stability during storage and facilitating selective reactions when needed. Its ability to remain chemically inert until activated makes it ideal for applications requiring controlled reactivity. These properties contribute to its widespread use in advanced chemical and biological studies.

In Indonesian laboratories, this compound is frequently used in biochemical and pharmacological research. Scientists rely on its stability and reactivity to develop new drugs and understand molecular interactions. Its availability in solid form and high purity make it suitable for both small-scale and more extensive laboratory experiments. The compound's resistance to degradation further supports its long-term storage and repeated use in research settings.

Peptide Synthesis: This compound is ideal for peptide synthesis due to its protective group that allows controlled coupling reactions and efficient peptide chain elongation.
Organic Chemistry Reactions: Its stability and reactivity make it suitable for a variety of organic reactions where functional group protection is essential.
Molecular Modification Studies: Researchers use it to modify complex molecules, enabling the study of structural changes and their biological implications.
Drug Development Research: It supports the development of new pharmaceutical compounds by facilitating the synthesis of bioactive molecules.
Biochemical Analysis: Its use in biochemical experiments helps in understanding enzyme interactions and molecular mechanisms in biological systems.

Brand	TCI
CAS number	73724-45-5
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from direct light

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to humidity, which could affect its stability. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is stable under normal storage conditions, it is advisable to avoid prolonged exposure to extreme temperatures. Proper labeling of containers is essential for safe handling and to prevent accidental contamination. Always ensure that the compound is stored in a secure location that is inaccessible to unauthorized personnel.

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