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Catalog Number:
30539
CAS Number:
1932033-81-2
Ácido ( 2R , 3R )-(Fmoc-amino)-3-(Boc-amino)butírico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Abu( 3R- Boc-Amino)-OH
Documents
$270.00 /100 mg
Tamaño
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Product Information

The compound (2R,3R)-(Fmoc-amino)-3-(Boc-amino)butyric acid is a versatile building block in peptide synthesis, particularly valued in the field of medicinal chemistry and biochemistry. This compound features both Fmoc (9-fluorenylmethoxycarbonyl) and Boc (tert-butyloxycarbonyl) protecting groups, which provide chemists with the flexibility to selectively deprotect amino acids during the synthesis of complex peptides. Its unique structure allows for the efficient assembly of peptides with desired sequences, making it an essential tool for researchers focused on drug development and protein engineering.

In addition to its role in peptide synthesis, this compound is also utilized in the development of various pharmaceuticals and biologically active molecules. Its stability under standard reaction conditions and compatibility with a range of coupling reagents enhance its appeal for both academic and industrial applications. Researchers can leverage this compound to streamline their workflows, improve yields, and achieve higher purity in their peptide products, ultimately accelerating the pace of discovery in therapeutic development.

Synonyms
Fmoc-D-Abu( 3R- Boc-Amino)-OH
CAS Number
1932033-81-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22989430
PubChem ID
14683495
Melting Point
152 - 158 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +27 ± 2º (C=0,5 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Abu( 3R- Boc-Amino)-OH
CAS Number
1932033-81-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD22989430
PubChem ID
14683495
Melting Point
152 - 158 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +27 ± 2º (C=0,5 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

(2R,3R)-(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, allowing researchers to create complex structures for various biological studies.
  • Drug Development: It plays a crucial role in the pharmaceutical industry, particularly in the design of new drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules for applications in diagnostics and targeted drug delivery systems, improving specificity and reducing side effects.
  • Research in Neuroscience: It is applied in the development of neuroactive compounds, aiding in the exploration of neurological disorders and potential treatments.
  • Protein Engineering: This compound is instrumental in modifying proteins to enhance their stability and functionality, which is essential in biotechnology and industrial applications.

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