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Catalog Number:
14486
CAS Number:
193693-62-8
Acide ( S )-(1-Fmoc-pipéridin-2-yl)acétique
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S )-Fmoc-(2-carboxyméthyl)pipéridine
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$86.23 /100 mg
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Product Information

(S)-(1-Fmoc-piperidin-2-yl)acetic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound, recognized for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, serves as an essential building block in the synthesis of peptides and other complex organic molecules. Its unique structure allows for selective reactions, making it invaluable for researchers focused on drug development and peptide synthesis. The compound's ability to facilitate the introduction of piperidine moieties enhances its utility in creating biologically active compounds, particularly in the pharmaceutical industry.

In addition to its role in peptide synthesis, (S)-(1-Fmoc-piperidin-2-yl)acetic acid is also employed in the development of various therapeutic agents. Its favorable properties, such as solubility and stability, make it an attractive choice for researchers looking to optimize their synthetic pathways. The compound's application extends to the design of novel ligands and inhibitors, showcasing its potential in advancing drug discovery efforts. With its robust profile, this compound stands out as a critical component for professionals aiming to innovate in the fields of biochemistry and pharmacology.

Synonyms
( S )-Fmoc-(2-carboxyméthyl)pipéridine
CAS Number
193693-62-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD06656476
PubChem ID
4712591
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +9,5 ± 1º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( S )-Fmoc-(2-carboxyméthyl)pipéridine
CAS Number
193693-62-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD06656476
PubChem ID
4712591
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +9,5 ± 1º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-(1-Fmoc-piperidin-2-yl)acetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, enhancing the efficiency and yield of the process.
  • Drug Development: It is used in the development of pharmaceuticals, especially in creating compounds that target specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The chemical's ability to form stable linkages with biomolecules makes it ideal for bioconjugation applications, which are essential in the development of targeted drug delivery systems.
  • Research in Neuroscience: Its structural properties allow researchers to explore its effects on neurotransmitter systems, contributing to studies on neuropharmacology and potential treatments for neurological disorders.
  • Analytical Chemistry: This compound is utilized in analytical methods for the detection and quantification of various biomolecules, providing reliable results in research and quality control settings.

Citations