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Catalog Number:
30541
CAS Number:
2381842-52-8
Ácido (2 S ,3 R )-(Fmoc-amino)-3-aliloxi-carbonilaminobutírico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Abu( 3R- Aloc-amino)-OH
Documents
$234.85 /25 mg
Tamaño
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Product Information

The compound (2S,3R)-(Fmoc-amino)-3-allyloxycarbonylaminobutyric acid is a versatile building block in peptide synthesis, particularly valued for its role in the development of complex peptide structures. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it ideal for use in solid-phase peptide synthesis. Its unique structure, which includes an allyloxycarbonyl group, enhances its reactivity, allowing for selective modifications that are crucial in the design of bioactive peptides and pharmaceuticals.

Researchers and industry professionals can leverage this compound in various applications, including drug development, where it serves as a precursor for synthesizing peptide-based therapeutics. Its ability to facilitate the introduction of functional groups makes it particularly useful in the creation of targeted delivery systems and in the exploration of peptide interactions in biological systems. The compound's favorable properties, such as its solubility and stability, further support its use in both academic research and industrial applications, providing a reliable option for those looking to innovate in peptide chemistry.

Synonyms
Fmoc-L-Abu( 3R- Aloc-amino)-OH
CAS Number
2381842-52-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.4
MDL Number
MFCD22989437
PubChem ID
75627324
Melting Point
165 - 172 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D20
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Abu( 3R- Aloc-amino)-OH
CAS Number
2381842-52-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.4
MDL Number
MFCD22989437
PubChem ID
75627324
Melting Point
165 - 172 ?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,3R)-(Fmoc-amino)-3-allyloxycarbonylaminobutyric 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 drug development.
  • Drug Delivery Systems: Its unique properties enable the formulation of advanced drug delivery systems, enhancing the bioavailability and targeting of therapeutic agents.
  • Bioconjugation: The chemical is used in bioconjugation techniques to attach biomolecules, facilitating the development of targeted therapies and diagnostic tools.
  • Research in Cancer Therapeutics: It plays a critical role in the development of novel cancer treatments by enabling the design of compounds that can selectively target cancer cells.
  • Protein Engineering: This compound is instrumental in protein engineering, allowing scientists to modify proteins for improved functionality and stability in various applications.

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