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Catalog Number:
29917
CAS Number:
1313054-60-2
Fmoc-N w -(2,2,4,6,7-pentaméthyl-dihydrobenzofuran-5-sulfonyl)-D-homoarginine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-D-HomoArg(Pbf)-OH
Documents
$50.00 /25 mg
Taille
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Product Information

Fmoc-N?-(2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyl)-D-homoarginine is a specialized compound designed for advanced applications in peptide synthesis and drug development. This compound features a unique sulfonyl group that enhances its reactivity and stability, making it an ideal choice for researchers focused on the synthesis of complex peptides and proteins. Its distinctive structure allows for improved solubility and bioavailability, which are critical factors in pharmaceutical formulations.

In the realm of biochemistry and medicinal chemistry, this compound serves as a valuable building block for the development of peptide-based therapeutics. Its ability to facilitate the introduction of specific functional groups into peptide sequences opens up new avenues for the design of targeted therapies. Researchers can leverage its properties to create innovative solutions in drug delivery systems, enhancing the efficacy of therapeutic agents. With its robust performance and versatility, this compound stands out as a key player in the ongoing evolution of peptide chemistry.

Synonyms
Fmoc-D-HomoArg(Pbf)-OH
CAS Number
1313054-60-2
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 35 H 42 N 4 O 7 S
Molecular Weight
662.8
MDL Number
MFCD15142012
PubChem ID
73995296
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-HomoArg(Pbf)-OH
CAS Number
1313054-60-2
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 35 H 42 N 4 O 7 S
Molecular Weight
662.8
MDL Number
MFCD15142012
PubChem ID
73995296
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-N?-(2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyl)-D-homoarginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, enhancing the efficiency of creating complex peptides with specific functionalities.
  • Drug Development: Its unique structure allows for the design of novel therapeutic agents, particularly in targeting specific biological pathways, making it valuable in pharmaceutical research.
  • Bioconjugation: The sulfonyl group facilitates bioconjugation processes, enabling the attachment of drugs or imaging agents to biomolecules, which is crucial in developing targeted therapies.
  • Research in Neuroscience: It can be used to study neuropeptide interactions, providing insights into neurological functions and potential treatments for neurodegenerative diseases.
  • Customizable Research Tools: Researchers can modify this compound to create tailored reagents for various biochemical assays, enhancing the versatility of experimental designs.

Citations