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Catalog Number:
30489
CAS Number:
1409939-21-4
Ácido ( R )-4-(Fmoc-amino)-3-(Boc-amino)butírico
Purity:
≥ 99% (Ensayo por titulación)
Synonym(s):
Ácido Nb-Boc-Ng-Fmoc-L-diaminobutírico, Boc-L-Dbu(Fmoc)-OH
Documents
$180.00 /100 mg
Tamaño
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Product Information

(R)-4-(Fmoc-amino)-3-(Boc-amino)butyric acid is a versatile amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features both Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butoxycarbonyl) protective groups, making it an excellent choice for the selective protection of amino functionalities during multi-step synthesis processes. Its unique structure allows for the efficient assembly of complex peptides, which are crucial in drug development and biological research.

Researchers appreciate this compound for its stability under various reaction conditions and its compatibility with a range of coupling reagents. The ability to easily remove the protective groups under mild conditions enhances its utility in synthesizing bioactive peptides and pharmaceutical intermediates. With applications spanning from academic research to industrial-scale peptide production, (R)-4-(Fmoc-amino)-3-(Boc-amino)butyric acid stands out as a reliable building block for innovative therapeutic solutions.

Synonyms
Ácido Nb-Boc-Ng-Fmoc-L-diaminobutírico, Boc-L-Dbu(Fmoc)-OH
CAS Number
1409939-21-4
Purity
≥ 99% (Ensayo por titulación)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22666113
PubChem ID
130145663
Melting Point
185 - 187 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 8 ± 1 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido Nb-Boc-Ng-Fmoc-L-diaminobutírico, Boc-L-Dbu(Fmoc)-OH
CAS Number
1409939-21-4
Purity
≥ 99% (Ensayo por titulación)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22666113
PubChem ID
130145663
Melting Point
185 - 187 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 8 ± 1 º (C=1 en DMF)
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

(R)-4-(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, particularly in solid-phase peptide synthesis (SPPS), allowing researchers to create complex peptides efficiently.
  • Drug Development: Its role in drug design is significant, as it can be used to develop peptide-based therapeutics, enhancing the efficacy and specificity of drug candidates.
  • Bioconjugation: The chemical is useful in bioconjugation processes, where it can help attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter function, as certain peptides derived from this compound can mimic or influence neurotransmitter activity.
  • Protein Engineering: This compound aids in the modification of proteins, allowing scientists to explore structure-function relationships and improve the stability and activity of therapeutic proteins.

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