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Catalog Number:
04795
CAS Number:
155369-11-2
Fmoc-(3-aminomethyl) benzoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-3-Amb-OH
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Product Information

Fmoc-(3-aminomethyl) benzoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for easy cleavage under mild conditions, making it an ideal choice for researchers looking to streamline their synthesis processes.

In addition to its role in peptide chemistry, Fmoc-(3-aminomethyl) benzoic acid is also valuable in the development of pharmaceutical intermediates and can serve as a building block for various bioactive compounds. Its compatibility with solid-phase peptide synthesis (SPPS) techniques enhances its appeal in the pharmaceutical industry, where efficiency and precision are paramount. Researchers and industry professionals can leverage this compound to improve yields and reduce reaction times, ultimately accelerating the development of new therapeutic agents.

Synonyms
Fmoc-3-Amb-OH
CAS Number
155369-11-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.41
MDL Number
MFCD00273463
PubChem ID
2756080
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-3-Amb-OH
CAS Number
155369-11-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.41
MDL Number
MFCD00273463
PubChem ID
2756080
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(3-aminomethyl) benzoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with the overall peptide structure.
  • Drug Development: It is used in the design of peptide-based drugs, enhancing the stability and bioavailability of therapeutic peptides in pharmaceutical formulations.
  • Bioconjugation: The chemical is effective in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and targeted drug delivery systems.
  • Research in Cancer Therapy: Its derivatives are explored in cancer research for their potential to improve the efficacy of chemotherapeutic agents by targeting specific cancer cells.
  • Materials Science: The compound is also investigated for its role in creating functionalized polymers, which can be used in advanced materials with tailored properties for various applications.

Citations