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Product Information

Product Name
Fmoc-(4-aminomethyl) benzoic acid
Brand Name
Chem Impex
Product Number
07315
CAS
164470-64-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2756083
IUPAC Name
4-(9H-fluoren-9-ylmethoxycarbonylamino)methylbenzoic acid
InChI Key
JRHUROPSUJVMNH-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCC4=CC=C(C=C4)C(=O)O

Application

Fmoc-(4-aminomethyl) benzoic acid is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.

Drug Development: In pharmaceutical research, it aids in the design of drug candidates by modifying amino acids, enhancing their bioavailability and therapeutic efficacy. This is crucial for developing effective treatments.

Bioconjugation: The compound is used to attach biomolecules to surfaces or other molecules, facilitating the creation of targeted drug delivery systems and improving the specificity of therapeutic agents.

Material Science: It finds applications in creating functional materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine, providing scaffolds that mimic natural tissues.

Analytical Chemistry: Researchers utilize this compound in chromatography and mass spectrometry for the separation and identification of complex mixtures, enhancing the accuracy of analytical methods.

References Data Source From Pubchem

Amide-Bond Formation

Publication Name: Science of Synthesis
Publication Date: 2024

Solid-Phase Synthesis of Trisubsituted Guanidines

Publication Name: Journal of Combinatorial Chemistry
Publication Date: 2002-02-09
DOI: 10.1021/cc0100621

Solid-supported syntheses of 3-thio-1,2,4-triazoles

Publication Name: Molecular Diversity
Publication Date: 1997-06
DOI: 10.1023/a:1009696119443