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Catalog Number:
41513
CAS Number:
1221793-43-6
(S)-1-Fmoc-4-oxopiperidine-2-carboxylic acid
Purity:
≥ 97%
Synonym(s):
(S)-1-Fmoc-4-oxohomoproline, Fmoc-L-Homopro(4-oxo)-OH
Hazmat
Documents
$129.19 /500MG
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Product Information
Synonyms
(S)-1-Fmoc-4-oxohomoproline, Fmoc-L-Homopro(4-oxo)-OH
CAS Number
1221793-43-6
Purity
≥ 97%
Molecular Formula
C21H19NO5
Molecular Weight
0
MDL Number
MFCD03094868
PubChem ID
75273738
Melting Point
228 - 233 °C
Appearance
Solid
Conditions
Store at 2 - 8 °C
General Information
Synonyms
(S)-1-Fmoc-4-oxohomoproline, Fmoc-L-Homopro(4-oxo)-OH
CAS Number
1221793-43-6
Purity
≥ 97%
Molecular Formula
C21H19NO5
Molecular Weight
0
MDL Number
MFCD03094868
PubChem ID
75273738
Melting Point
228 - 233 °C
Appearance
Solid
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-1-Fmoc-4-oxopiperidine-2-carboxylic 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 the development of pharmaceuticals and biologically active compounds.
  • Drug Development: It plays a crucial role in the design and synthesis of novel drug candidates, especially in the field of medicinal chemistry, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, allowing researchers to attach biomolecules to drugs, improving targeted delivery systems in cancer therapy.
  • Research in Neuroscience: Its derivatives are studied for their potential neuroprotective effects, contributing to advancements in treatments for neurodegenerative diseases.
  • Material Science: This compound is also explored in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties.

Citations