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Catalog Number:
29667
CAS Number:
1076197-06-2
Fmoc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Documents
$86.23 /100MG
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Product Information

Fmoc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This compound features a fluorinated phenyl group that enhances its reactivity and selectivity, making it an excellent choice for researchers looking to develop novel peptides with improved pharmacological properties. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating the synthesis of complex peptide structures.

In addition to its application in peptide synthesis, Fmoc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid serves as a valuable intermediate in the development of pharmaceuticals, particularly in the design of inhibitors and receptor ligands. The unique combination of the piperidine ring and the fluorinated aromatic system provides enhanced lipophilicity and bioavailability, making it an attractive candidate for drug development. Researchers can leverage its properties to create compounds with targeted therapeutic effects, thereby advancing the field of drug discovery.

CAS Number
1076197-06-2
Purity
≥ 99% (HPLC)
Molecular Formula
C27H24FNO4
Molecular Weight
445.49
MDL Number
MFCD11226817
PubChem ID
45356724
Melting Point
177-183 ºC
Appearance
White Powder
Conditions
Store at 0-8°C
General Information
CAS Number
1076197-06-2
Purity
≥ 99% (HPLC)
Molecular Formula
C27H24FNO4
Molecular Weight
445.49
MDL Number
MFCD11226817
PubChem ID
45356724
Melting Point
177-183 ºC
Appearance
White Powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial for researchers developing new therapeutic peptides.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in the development of compounds targeting specific receptors in the body, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used in bioconjugation techniques, linking biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics.
  • Material Science: In polymer chemistry, it can be utilized to create functionalized polymers with specific properties, beneficial for developing advanced materials in various applications, including coatings and adhesives.
  • Research in Neuroscience: Its structural features make it a valuable tool in studying neuropharmacology, helping researchers understand the interactions between drugs and neural pathways.

Citations