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Catalog Number:
30540
CAS Number:
370865-67-1, 131669-43-7
Ácido (2 S ,3 S )-(Fmoc-amino)-3-(Boc-amino)butírico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Abu( 3S- Boc-Amino)-OH
Documents
$134.70 /25 mg
Tamaño
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Product Information

(2S,3S)-(Fmoc-amino)-3-(Boc-amino)butyric acid is a versatile building block in peptide synthesis, widely utilized in the field of medicinal chemistry and biochemistry. This compound features both Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) protecting groups, making it an ideal choice for the protection of amino acids during solid-phase peptide synthesis. Its unique structure allows for the selective deprotection of functional groups, facilitating the assembly of complex peptides with high purity and yield. Researchers appreciate its stability under various conditions, which enhances its usability in diverse applications, from drug development to the creation of bioconjugates.

In addition to its role in peptide synthesis, (2S,3S)-(Fmoc-amino)-3-(Boc-amino)butyric acid can be employed in the development of peptide-based therapeutics and vaccines. Its ability to form stable linkages and its compatibility with various coupling reagents make it a valuable asset in the design of novel biomolecules. This compound stands out due to its dual protection strategy, allowing for greater flexibility and efficiency in synthetic pathways compared to other amino acid derivatives.

Synonyms
Fmoc-L-Abu( 3S- Boc-Amino)-OH
CAS Number
370865-67-1, 131669-43-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22989431
PubChem ID
14683495
Melting Point
151-158 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D20
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Abu( 3S- Boc-Amino)-OH
CAS Number
370865-67-1, 131669-43-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22989431
PubChem ID
14683495
Melting Point
151-158 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D20
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,3S)-(Fmoc-amino)-3-(Boc-amino)butyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are vital in drug development and biological research.
  • Drug Development: It plays a significant role in the design of novel therapeutics, particularly in creating peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: Used in bioconjugation processes, it aids in attaching biomolecules to surfaces or other molecules, enhancing the functionality of diagnostics and therapeutics.
  • Research in Neuroscience: This compound is employed in studies related to neuropeptides, helping researchers understand neurological functions and disorders.
  • Custom Synthesis Services: It is often utilized by contract research organizations (CROs) for custom synthesis, allowing for tailored solutions in pharmaceutical and biotech industries.

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