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Catalog Number:
30485
CAS Number:
763102-80-3
Ácido ( R )-4-(Boc-amino)-3-(Fmoc-amino)butírico
Purity:
≥ 99% (ensayo por titulación, HPLC)
Synonym(s):
Fmoc-L-Dbu(Boc)-OH
Documents
$75.00 /100 mg
Tamaño
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Product Information

(R)-4-(Boc-amino)-3-(Fmoc-amino)butyric acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique combination of protective groups, namely the Boc (tert-butyloxycarbonyl) and Fmoc (9-fluorenylmethoxycarbonyl), which facilitate selective reactions and enhance the stability of intermediates during synthesis. Its chiral center allows for the production of enantiomerically pure compounds, making it particularly valuable in the pharmaceutical industry where stereochemistry is crucial for drug efficacy.

Researchers and industry professionals can leverage (R)-4-(Boc-amino)-3-(Fmoc-amino)butyric acid in the development of complex peptides and biologically active molecules. Its ability to protect amino groups while allowing for further functionalization makes it an essential building block in the synthesis of therapeutic peptides. This compound not only streamlines the synthesis process but also improves yields and purity, providing a significant advantage over similar compounds in the market.

Synonyms
Fmoc-L-Dbu(Boc)-OH
CAS Number
763102-80-3
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22666112
PubChem ID
66785279
Melting Point
155 - 160 °C (descenso)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 9 ± 1 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Dbu(Boc)-OH
CAS Number
763102-80-3
Purity
≥ 99% (ensayo por titulación, HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22666112
PubChem ID
66785279
Melting Point
155 - 160 °C (descenso)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 9 ± 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-(Boc-amino)-3-(Fmoc-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, enabling researchers to create complex molecules for drug development and therapeutic applications.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for designing and optimizing drug candidates, particularly in the development of targeted therapies.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, contributing to the understanding of neurological pathways and potential treatments for neurodegenerative diseases.
  • Custom Synthesis Services: Many contract research organizations utilize this compound to provide tailored synthesis solutions for clients, addressing specific research needs and challenges.

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