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Catalog Number:
05047
CAS Number:
959572-93-1
Fmoc-5-aminomethyl-2,3-O-isopropylidene-α-L-xylo-3-hexolofuranosonic aicd
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-Aixa-OH
Documents
$234.85 /100MG
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Product Information

Fmoc-5-aminomethyl-2,3-O-isopropylidene-a-L-xylo-3-hexolofuranosonic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound, characterized by its unique structure, serves as an essential building block for the development of glycosylated compounds, which are crucial in the synthesis of various biologically active molecules. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for peptide synthesis and other applications where controlled reactivity is desired.

Researchers and industry professionals can leverage this compound in the design of glycoproteins and carbohydrate-based therapeutics, enhancing the efficacy of drug delivery systems. Its stability and compatibility with various reaction conditions further underscore its utility in complex organic transformations. With its ability to facilitate the synthesis of novel compounds, Fmoc-5-aminomethyl-2,3-O-isopropylidene-a-L-xylo-3-hexolofuranosonic acid stands out as a valuable asset in both academic research and pharmaceutical development.

Synonyms
Fmoc-Aixa-OH
CAS Number
959572-93-1
Purity
≥ 97% (HPLC)
Molecular Formula
C24H25NO8
Molecular Weight
455.43
MDL Number
MFCD08458511
PubChem ID
4712608
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -14 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-Aixa-OH
CAS Number
959572-93-1
Purity
≥ 97% (HPLC)
Molecular Formula
C24H25NO8
Molecular Weight
455.43
MDL Number
MFCD08458511
PubChem ID
4712608
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -14 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-5-aminomethyl-2,3-O-isopropylidene-a-L-xylo-3-hexolofuranosonic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting others. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: Its unique structure aids in the development of glycosylated drugs, which can enhance the efficacy and specificity of therapeutic agents, particularly in targeting specific cells or tissues.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to drugs or imaging agents, which is essential in developing targeted therapies and diagnostic tools.
  • Glycobiology Research: It plays a significant role in glycobiology, helping researchers study carbohydrate-protein interactions, which are vital for understanding various biological processes and disease mechanisms.
  • Material Science: The compound can be incorporated into polymer systems to create materials with specific properties, such as enhanced biocompatibility or controlled release characteristics, beneficial for medical implants and drug delivery systems.

Citations