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Catalog Number:
03960
CAS Number:
123417-19-6
Ester β-9-fluorénylméthylique de l'acide boc-D-aspartique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-Asp(OFm)-OH
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Product Information

Boc-D-aspartic acid b-9-fluorenylmethyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected form of D-aspartic acid features a Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for various applications in organic chemistry. Its unique structure allows for selective reactions, facilitating the development of complex peptides and bioactive molecules. Researchers often leverage this compound in the synthesis of neuropeptides and other biologically active substances, contributing to advancements in drug discovery and development.

The compound's ability to protect the amino group while maintaining reactivity at the carboxylic acid site makes it particularly valuable in solid-phase peptide synthesis. Its application extends to the creation of peptide-based therapeutics, where precise control over amino acid sequences is crucial. By incorporating Boc-D-aspartic acid b-9-fluorenylmethyl ester into their workflows, chemists can enhance the efficiency and yield of their synthetic processes, ultimately leading to innovative solutions in medicinal chemistry and biotechnology.

Synonyms
Boc-D-Asp(OFm)-OH
CAS Number
123417-19-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.5
MDL Number
MFCD00151867
PubChem ID
14308456
Melting Point
139 - 141 °C
Appearance
Poudre blanche
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-D-Asp(OFm)-OH
CAS Number
123417-19-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.5
MDL Number
MFCD00151867
PubChem ID
14308456
Melting Point
139 - 141 °C
Appearance
Poudre blanche
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

Boc-D-aspartic acid b-9-fluorenylmethyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This chemical serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological functions.
  • Drug Development: Its derivatives are explored in pharmaceutical research for developing new drugs, particularly in targeting neurological disorders due to its amino acid properties.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Research in Neuroscience: The compound is valuable in studies related to neurotransmission and receptor interactions, providing insights into brain function and potential treatments.
  • Custom Synthesis: Researchers often utilize this compound for custom synthesis projects, where specific modifications are needed for unique applications in various fields.

Citations