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Catalog Number:
15021
CAS Number:
959584-22-6
N-(1-Boc-piperidin-4-yl)-L-aspartic acid-4-benzyl ester
Purity:
≥ 97% (HPLC)
Documents
$174.96 /250MG
Pack Size Availability Price
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Product Information

N-(1-Boc-piperidin-4-yl)-L-aspartic acid-4-benzyl ester is a versatile compound widely utilized in pharmaceutical research and development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an excellent candidate for peptide synthesis and drug formulation. Its unique structure allows for effective interactions with biological targets, facilitating the development of novel therapeutics. Researchers have found this compound particularly useful in the synthesis of bioactive peptides and as a building block in medicinal chemistry, where it can be employed to create compounds with enhanced pharmacological properties.

In addition to its applications in drug discovery, N-(1-Boc-piperidin-4-yl)-L-aspartic acid-4-benzyl ester serves as a valuable tool in the study of receptor interactions and enzyme inhibition. Its ability to mimic natural substrates makes it an essential component in the design of inhibitors for various biological pathways. The compound's favorable characteristics, including its stability and ease of modification, position it as a preferred choice for researchers aiming to explore new therapeutic avenues and optimize drug efficacy.

CAS Number
959584-22-6
Purity
≥ 97% (HPLC)
Molecular Formula
C21H30N2O6
Molecular Weight
406.48
MDL Number
MFCD04112673
PubChem ID
4712513
Appearance
White amorphous powder
Optical Rotation
[a]D20 = +13 ± 2º (C=1 in AcOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
959584-22-6
Purity
≥ 97% (HPLC)
Molecular Formula
C21H30N2O6
Molecular Weight
406.48
MDL Number
MFCD04112673
PubChem ID
4712513
Appearance
White amorphous powder
Optical Rotation
[a]D20 = +13 ± 2º (C=1 in AcOH)
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

N-(1-Boc-piperidin-4-yl)-L-aspartic acid-4-benzyl ester is widely utilized in research focused on:

  • Drug Development: This compound serves as a versatile building block in the synthesis of novel pharmaceuticals, particularly in the development of neuroprotective agents and treatments for neurological disorders.
  • Peptide Synthesis: It is employed in the synthesis of peptides, enhancing the stability and bioavailability of therapeutic peptides by providing a protective group that can be easily removed during the final stages of synthesis.
  • Bioconjugation: The compound can be used in bioconjugation processes, allowing researchers to attach drugs or imaging agents to biomolecules, which is crucial in targeted drug delivery systems.
  • Research in Neuroscience: Its structural properties make it a valuable tool in neuroscience research, particularly in studying receptor interactions and signaling pathways related to neurotransmitters.
  • Custom Synthesis: The compound is favored in custom synthesis projects for laboratories, providing a reliable option for researchers looking to create specific derivatives for various applications.

Citations