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Catalog Number:
22741
CAS Number:
369403-24-7
Fmoc-8-amino-1,4-dioxa-spiro[4,5]decane-8-carboxylic acid
Purity:
≥ 98% (HPLC)
Documents
$134.70 /100MG
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Product Information

Fmoc-8-amino-1,4-dioxa-spiro[4,5]decane-8-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique spiro structure that enhances its stability and reactivity, making it an ideal choice for researchers focused on developing complex peptides and biologically active molecules. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of peptides with high purity and yield.

In addition to its applications in peptide synthesis, this compound is also valuable in the field of medicinal chemistry, where it can be employed to create novel drug candidates. Its distinctive structure and functional groups enable researchers to explore various modifications, potentially leading to the discovery of new therapeutic agents. The compound's ability to form stable linkages and its compatibility with various coupling reagents further enhance its utility in laboratory settings, making it a preferred choice for professionals in academia and industry alike.

CAS Number
369403-24-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO6
Molecular Weight
423.46
MDL Number
MFCD02683159
PubChem ID
1268221
Melting Point
133-144 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
CAS Number
369403-24-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H25NO6
Molecular Weight
423.46
MDL Number
MFCD02683159
PubChem ID
1268221
Melting Point
133-144 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Fmoc-8-amino-1,4-dioxa-spiro[4,5]decane-8-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation strategies, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is employed in the synthesis of neuropeptides, aiding in the study of neurological pathways and potential treatments for neurodegenerative diseases.
  • Material Science: The compound can be utilized in developing advanced materials with specific properties, such as hydrophilicity or biocompatibility, which are important in biomedical applications.

Citations