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Catalog Number:
14484
CAS Number:
193693-63-9
R-(1-Fmoc-piperidin-2-yl)acetic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
(R-Fmoc-(2-carboxymethyl)piperidine
Documents
$58.39 /25MG
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Product Information

(R)-(1-Fmoc-piperidin-2-yl)acetic acid is a versatile compound widely utilized in the fields of medicinal chemistry and peptide synthesis. This compound serves as an essential building block for the development of various pharmaceuticals, particularly in the synthesis of peptide-based drugs. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for researchers looking to streamline their synthetic pathways.

In addition to its role in peptide synthesis, (R)-(1-Fmoc-piperidin-2-yl)acetic acid is also valuable in the development of ligands and other bioactive molecules. Its chiral nature enhances its relevance in asymmetric synthesis, providing researchers with the ability to create compounds with specific stereochemical configurations. This compound is particularly beneficial for those working in drug discovery and development, as it facilitates the creation of complex molecules with high precision.

Synonyms
(R-Fmoc-(2-carboxymethyl)piperidine
CAS Number
193693-63-9
Purity
≥ 99% (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD06656475
PubChem ID
4712591
Appearance
White powder
Optical Rotation
-9.0 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
(R-Fmoc-(2-carboxymethyl)piperidine
CAS Number
193693-63-9
Purity
≥ 99% (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD06656475
PubChem ID
4712591
Appearance
White powder
Optical Rotation
-9.0 ± 2º (C=1 in DMF)
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

(R)-(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: Its unique structure allows for the modification of drug candidates, aiding in the development of pharmaceuticals with improved efficacy and reduced side effects.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in targeted drug delivery systems, improving the precision of therapeutic agents.
  • Research in Neuroscience: It is utilized in studies involving neurotransmitter pathways, providing insights into neurological disorders and potential treatments.
  • Analytical Chemistry: This chemical is employed in various analytical techniques, such as HPLC, to separate and identify complex mixtures, ensuring high-quality results in research and industry applications.

Citations