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Catalog Number:
05487
CAS Number:
123417-20-9
Éster γ-9-fluorenilmetílico del ácido Boc-D-glutámico
Purity:
≥ 99 % (HPLC, TLC)
Synonym(s):
Boc-D-Glu(OFm)-OH, Éster 5-(9-fluorenilmetil) del ácido Boc-D-glutámico
Documents
$113.87 /1G
Tamaño
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Product Information

Boc-D-glutamic acid g-9-fluorenylmethyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a Boc (tert-butyloxycarbonyl) group, which provides stability and enhances the compound's solubility, making it an ideal choice for researchers engaged in the synthesis of complex peptides. Its unique structure, characterized by the 9-fluorenylmethyl ester, allows for selective deprotection under mild conditions, facilitating the efficient assembly of peptide chains.

In the pharmaceutical industry, Boc-D-glutamic acid g-9-fluorenylmethyl ester serves as a crucial building block in the design of bioactive peptides and therapeutic agents. Its applications extend to the development of targeted drug delivery systems and the creation of novel biomaterials. Researchers appreciate its compatibility with various coupling reagents and its ability to enhance the stability and bioavailability of peptide-based drugs. With its favorable properties and practical applications, this compound is an essential tool for professionals in medicinal chemistry and peptide research.

Synonyms
Boc-D-Glu(OFm)-OH, Éster 5-(9-fluorenilmetil) del ácido Boc-D-glutámico
CAS Number
123417-20-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C24H27Nº6
Molecular Weight
425.5
MDL Number
MFCD00151871
PubChem ID
4712641
Melting Point
115 - 121 °C
Appearance
Polvo blanco
Optical Rotation
[a] 20 D
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D-Glu(OFm)-OH, Éster 5-(9-fluorenilmetil) del ácido Boc-D-glutámico
CAS Number
123417-20-9
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C24H27Nº6
Molecular Weight
425.5
MDL Number
MFCD00151871
PubChem ID
4712641
Melting Point
115 - 121 °C
Appearance
Polvo blanco
Optical Rotation
[a] 20 D
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-D-glutamic acid g-9-fluorenylmethyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its protective group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In medicinal chemistry, it is used to create compounds with potential therapeutic effects. Researchers leverage its structure to design drugs targeting various diseases, including neurological disorders.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for their potential to modulate neurotransmitter systems, aiding in the understanding of brain function and the development of treatments for mental health conditions.
  • Analytical Chemistry: It is utilized in analytical methods to study protein interactions and stability, providing insights that are critical for both academic research and industrial applications.

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