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Catalog Number:
23928
CAS Number:
1212405-65-6
Acide S -2-(((9 H -Fluoren-9-yl)méthoxy)carbonylamino)-3-(1,3-dioxoisoindolin-2-yl)propanoïque
Purity:
≥ 98 % (HPLC)
Documents
$312.27 /100 mg
Taille
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Product Information

(S)-2-(((9H-Fluoren-9-yl)methoxy)carbonylamino)-3-(1,3-dioxoisoindolin-2-yl)propanoic acid is a sophisticated compound that plays a vital role in the field of organic synthesis and pharmaceutical development. This compound, often referred to as Fmoc-3-(1,3-dioxoisoindolin-2-yl)propanoic acid, is particularly valuable for researchers engaged in peptide synthesis and drug discovery. Its unique structure allows for the selective modification of amino acids, making it an essential building block in the creation of complex peptides and proteins.

The compound's dioxoisoindoline moiety enhances its reactivity, facilitating the formation of peptide bonds under mild conditions. This feature is advantageous for researchers looking to develop novel therapeutics with improved efficacy and reduced side effects. Additionally, its fluorenylmethoxycarbonyl (Fmoc) protecting group provides stability during synthesis, allowing for greater control over reaction conditions. This compound is ideal for applications in medicinal chemistry, particularly in the design of targeted therapies and biologically active compounds.

CAS Number
1212405-65-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H20N2O6
Molecular Weight
456.45
MDL Number
MFCD09910433
PubChem ID
75192756
Appearance
Solide blanc
Optical Rotation
[a] 20 D = -83,4 ± 2 ° (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
1212405-65-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H20N2O6
Molecular Weight
456.45
MDL Number
MFCD09910433
PubChem ID
75192756
Appearance
Solide blanc
Optical Rotation
[a] 20 D = -83,4 ± 2 ° (C=1 dans MeOH)
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

(S)-2-(((9H-Fluoren-9-yl)methoxy)carbonylamino)-3-(1,3-dioxoisoindolin-2-yl)propanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, enhancing the efficiency of creating complex peptides by preventing unwanted reactions during the process.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for designing and developing new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to various surfaces, which is essential in diagnostics and therapeutics.
  • Analytical Chemistry: It is employed as a standard in analytical methods, aiding in the accurate quantification of similar compounds in complex mixtures.
  • Material Science: This chemical is explored in the development of novel materials, particularly those with specific optical or electronic properties, benefiting industries like electronics and coatings.

Citations