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Catalog Number:
03739
CAS Number:
210754-59-9
2 S ,3 S -Fmoc-Apns-OH
Purity:
≥ 97 % (HPLC)
Synonym(s):
Acide Fmoc-(2 S ,3 S -3-amino-2-hydroxy-4-phénylbutyrique, 2 S, 3 S -Fmoc-AHPBA
Documents
$141.41 /100 mg
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Product Information

The compound (2S,3S)-Fmoc-Apns-OH, also known as Fmoc-2-amino-3-hydroxy-4-phenylbutanoic acid, is a valuable building block in peptide synthesis and medicinal chemistry. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection, making it an ideal choice for synthesizing complex peptides and proteins. Researchers and industry professionals utilize this compound for its ability to enhance the stability and solubility of peptides, facilitating the development of therapeutic agents and biologically active molecules.

In addition to its role in peptide synthesis, (2S,3S)-Fmoc-Apns-OH has shown potential in drug discovery and development, particularly in the creation of novel compounds with specific biological activities. Its application in combinatorial chemistry and high-throughput screening further underscores its importance in pharmaceutical research. By incorporating this compound into their workflows, researchers can streamline the synthesis process, improve yields, and explore new avenues in drug design, ultimately leading to innovative solutions in healthcare.

Synonyms
Acide Fmoc-(2 S ,3 S -3-amino-2-hydroxy-4-phénylbutyrique, 2 S, 3 S -Fmoc-AHPBA
CAS Number
210754-59-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C 25 H 235
Molecular Weight
417.46
MDL Number
MFCD00467714
PubChem ID
4712585
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -27 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide Fmoc-(2 S ,3 S -3-amino-2-hydroxy-4-phénylbutyrique, 2 S, 3 S -Fmoc-AHPBA
CAS Number
210754-59-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C 25 H 235
Molecular Weight
417.46
MDL Number
MFCD00467714
PubChem ID
4712585
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -27 ± 1 ° (C = 1 dans DMF)
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

(2S,3S)-Fmoc-Apns-OH is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create custom peptides for various applications in drug development and biochemistry.
  • Drug Development: Its role in modifying amino acids makes it valuable in the pharmaceutical industry for designing new therapeutic agents, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics in biomedical applications.
  • Research in Protein Engineering: It aids in the study of protein structures and functions, enabling scientists to explore new protein designs and their interactions in biological systems.
  • Analytical Chemistry: The compound is employed in various analytical techniques, such as chromatography, to separate and identify complex mixtures, proving essential for quality control in laboratories.

Citations