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Catalog Number:
10545
CAS Number:
183673-66-7
1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Pip(Boc)-OH, 1-Boc-4-Fmoc-Pip-OH
Documents
$72.31 /250MG
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Product Information

1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a piperidine ring, which enhances its stability and reactivity, making it an excellent choice for researchers focused on developing novel therapeutics. Its unique structure, incorporating both Boc and Fmoc protecting groups, allows for selective deprotection, facilitating the stepwise assembly of complex peptides. This property is particularly beneficial in the synthesis of bioactive peptides and pharmaceuticals, where precision and efficiency are paramount.

In addition to its applications in peptide synthesis, 1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid serves as a valuable building block in the development of drug candidates targeting various diseases. Its ability to form stable linkages and maintain structural integrity under various conditions makes it an ideal candidate for researchers aiming to optimize drug delivery systems. The compound's favorable solubility and compatibility with various solvents further enhance its utility in laboratory settings, ensuring that it meets the rigorous demands of modern chemical research.

Synonyms
Fmoc-L-Pip(Boc)-OH, 1-Boc-4-Fmoc-Pip-OH
CAS Number
183673-66-7
Purity
≥ 99% (HPLC)
Molecular Formula
C26H30N2O6
Molecular Weight
466.53
MDL Number
MFCD01318741
PubChem ID
2734399
Appearance
White to off-white solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Pip(Boc)-OH, 1-Boc-4-Fmoc-Pip-OH
CAS Number
183673-66-7
Purity
≥ 99% (HPLC)
Molecular Formula
C26H30N2O6
Molecular Weight
466.53
MDL Number
MFCD01318741
PubChem ID
2734399
Appearance
White to off-white solid
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

1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological activities.
  • Drug Development: Its unique functional groups enable the design of novel pharmaceuticals, particularly in the development of targeted therapies for various diseases.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the creation of bioconjugates for diagnostic and therapeutic applications.
  • Research in Neuroscience: Due to its piperidine structure, it is valuable in studying neurotransmitter systems and developing potential treatments for neurological disorders.
  • Material Science: The compound can be incorporated into polymers or coatings, enhancing the properties of materials used in various industrial applications.

Citations