4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]aminomethyl]benzoic Acid TCI F0925

Chemical Identity

Other names: 4-(Fmoc-aminomethyl)benzoic Acid
CAS No.: 164470-64-8
PubChem: CID 2756083·SID 253661682
Formula: C23H19NO4
Molecular weight: 373.41 g/mol
Purity: >98.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-[(9H-fluoren-9-ylmethoxycarbonylamino)methyl]benzoic acid
SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCC4=CC=C(C=C4)C(=O)O
InChIKey: JRHUROPSUJVMNH-UHFFFAOYSA-N
MDL: MDL01074693

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4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]aminomethyl]benzoic Acid is a complex chemical compound widely used in peptide chemistry and molecular synthesis. This material plays a crucial role in laboratory settings where the formation of peptide bonds is required. Its unique structure enables it to react with amines or amino acids, facilitating the synthesis of complex molecules with high structural specificity. It is an essential reagent for researchers working on advanced chemical biology projects, particularly those involving the modification of molecular structures.

The compound is favored for its ability to form amide bonds with amino groups, making it highly reactive in controlled chemical environments. Its fluoren-9-ylmethoxy carbonyl structure contributes to its stability and reactivity, allowing for efficient chemical transformations. The compound also exhibits good solubility in organic solvents, which simplifies purification and separation processes in the lab. These properties make it a reliable and versatile choice for a wide range of synthetic applications.

In Indonesian laboratories, this compound is commonly used by researchers in the fields of chemical biology and pharmaceutical sciences. It is frequently employed in the development of complex organic molecules and peptide-based compounds. Its availability and performance have made it a preferred material for academic and industrial research in Indonesia, supporting the advancement of chemical synthesis techniques.

TCI brochures (PDF)

Amino Acids and Peptide Synthesis Reagents 2025-08-14 · p. 21

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its ability to form stable amide bonds with amino groups, enabling the construction of complex peptide sequences.
Molecular Modification: It is used in molecular modification processes where specific structural changes are required, allowing for the creation of novel chemical entities.
Organic Chemistry Research: Its reactivity and stability make it a valuable tool in organic chemistry research, supporting the development of new compounds and reaction mechanisms.
Drug Development: The compound is utilized in drug development to create molecules with desired biological activities, particularly in the pharmaceutical industry.
Structural Chemistry Studies: It is employed in structural chemistry studies to investigate the behavior of complex molecules under various reaction conditions.

Brand	TCI
CAS number	164470-64-8
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various pack sizes as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during use. Due to its reactivity, it should be stored separately from strong acids or bases to avoid unwanted chemical interactions. Proper labeling of storage containers is essential to prevent misidentification and ensure safe handling. Regular monitoring of storage conditions is advised to maintain the compound’s stability and effectiveness for research applications.

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