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Catalog Number:
15078
CAS Number:
372159-75-6
Fmoc-3-amino-2-naphthoic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-3-aminonaphthalene-2-carboxylic acid
Documents
$79.22 /1G
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Product Information

Fmoc-3-amino-2-naphthoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an essential reagent in the production of complex peptides and proteins. Researchers appreciate its stability under various conditions, which enhances its reliability in laboratory settings.

In addition to its role in peptide synthesis, Fmoc-3-amino-2-naphthoic acid has applications in the development of pharmaceuticals, particularly in the design of novel therapeutic agents. Its naphthalene moiety contributes to the compound's hydrophobic characteristics, which can improve the bioavailability of drug candidates. This compound is particularly valuable in medicinal chemistry and biochemistry, where it aids in the exploration of new drug formulations and therapeutic strategies. With its proven efficacy and adaptability, Fmoc-3-amino-2-naphthoic acid stands out as a key reagent for professionals in the chemical and pharmaceutical industries.

Synonyms
Fmoc-3-aminonaphthalene-2-carboxylic acid
CAS Number
372159-75-6
Purity
≥ 97% (HPLC)
Molecular Formula
C26H19NO4
Molecular Weight
409.44
MDL Number
MFCD02682310
PubChem ID
17040109
Melting Point
225-237 °C
Appearance
Yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-3-aminonaphthalene-2-carboxylic acid
CAS Number
372159-75-6
Purity
≥ 97% (HPLC)
Molecular Formula
C26H19NO4
Molecular Weight
409.44
MDL Number
MFCD02682310
PubChem ID
17040109
Melting Point
225-237 °C
Appearance
Yellow 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-amino-2-naphthoic 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 affecting the overall structure.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in enhancing the bioavailability and stability of drug candidates.
  • Fluorescent Probes: Its unique structure makes it suitable for developing fluorescent probes used in biological imaging, helping researchers visualize cellular processes.
  • Material Science: The compound is used in creating advanced materials, such as polymers and nanomaterials, that require specific functional groups for enhanced properties.
  • Bioconjugation: It facilitates the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies and diagnostics in the biomedical field.

Citations