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Catalog Number:
29670
CAS Number:
1310680-48-8
Fmoc-4-(naphthalen-2-yl)-piperidine-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Documents
$113.87 /25MG
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Product Information

Fmoc-4-(naphthalen-2-yl)-piperidine-4-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its naphthalene moiety enhances the compound's hydrophobic interactions, making it particularly useful in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability under various conditions, which facilitates streamlined synthesis processes and improved yields.

In practical applications, Fmoc-4-(naphthalen-2-yl)-piperidine-4-carboxylic acid serves as a crucial building block in the development of peptide-based therapeutics, including those targeting cancer and neurological disorders. Its ability to form stable peptide bonds allows for the creation of complex peptide sequences that can be tailored for specific biological activities. Additionally, this compound's favorable solubility and reactivity profile make it an ideal choice for researchers looking to innovate in drug design and development.

CAS Number
1310680-48-8
Purity
≥ 99% (HPLC)
Molecular Formula
C31H27NO4
Molecular Weight
477.56
MDL Number
MFCD12408088
PubChem ID
74892117
Appearance
Off-white Powder
Conditions
Store at 0-8°C
General Information
CAS Number
1310680-48-8
Purity
≥ 99% (HPLC)
Molecular Formula
C31H27NO4
Molecular Weight
477.56
MDL Number
MFCD12408088
PubChem ID
74892117
Appearance
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-4-(naphthalen-2-yl)-piperidine-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceutical compounds, particularly in developing drugs targeting specific receptors in the central nervous system.
  • Bioconjugation: The compound can be used to create bioconjugates, linking biomolecules like proteins and antibodies to enhance their therapeutic efficacy.
  • Fluorescent Probes: Its naphthalene moiety can be utilized in the development of fluorescent probes for biological imaging, providing insights into cellular processes.
  • Material Science: The compound's properties make it suitable for creating advanced materials, such as polymers with tailored functionalities for applications in electronics and coatings.

Citations