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Catalog Number:
22722
CAS Number:
1217646-18-8
Acide S- (1-Fmoc-pipéridin-3-yl)acétique
Purity:
≥ 99 % (HPLC)
Synonym(s):
( S -Fmoc-(3-carboxyméthyl)pipéridine
Documents
$113.87 /25 mg
Taille
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Product Information

(S)-(1-Fmoc-piperidin-3-yl)acetic acid is a versatile compound widely utilized in the field of medicinal chemistry and peptide synthesis. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, plays a crucial role in the synthesis of peptides and other bioactive molecules. Its unique structure allows for selective deprotection, making it an invaluable tool for researchers looking to develop complex peptide sequences with high specificity and efficiency.

In addition to its applications in peptide synthesis, (S)-(1-Fmoc-piperidin-3-yl)acetic acid is also explored in drug discovery and development, particularly in the design of novel therapeutics targeting various biological pathways. Its ability to facilitate the introduction of piperidine moieties into molecular frameworks enhances the pharmacological properties of compounds, making it a preferred choice among chemists and pharmaceutical researchers. With its robust profile and practical applications, this compound stands out as a key ingredient in advancing drug development and therapeutic innovation.

Synonyms
( S -Fmoc-(3-carboxyméthyl)pipéridine
CAS Number
1217646-18-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD09264215
PubChem ID
4251851
Appearance
Poudre blanche
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8°C
General Information
Synonyms
( S -Fmoc-(3-carboxyméthyl)pipéridine
CAS Number
1217646-18-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD09264215
PubChem ID
4251851
Appearance
Poudre blanche
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-(1-Fmoc-piperidin-3-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, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: It plays a significant role in medicinal chemistry, where it is used to design and develop new pharmaceutical compounds, especially those targeting neurological disorders.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter systems, helping researchers understand the mechanisms of action of various neurological drugs.
  • Analytical Chemistry: This chemical is utilized in analytical methods for characterizing complex mixtures, providing insights into the composition and concentration of various compounds in a sample.

Citations