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Catalog Number:
14462
CAS Number:
959573-04-7
Ácido R -Fmoc-4-amino-5-(4- terc -butoxifenil)pentanoico
Purity:
≥ 98 % (HPLC)
Documents
$100.05 /25 mg
Tamaño
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Product Information

(R)-Fmoc-4-amino-5-(4-tert-butoxyphenyl)pentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the presence of a tert-butoxyphenyl moiety, enhances its stability and solubility, making it an ideal choice for researchers working in the fields of medicinal chemistry and biochemistry.

In practical applications, (R)-Fmoc-4-amino-5-(4-tert-butoxyphenyl)pentanoic acid serves as a key intermediate in the synthesis of bioactive peptides and pharmaceuticals. Its ability to facilitate the formation of peptide bonds while maintaining high purity levels is crucial for producing compounds with specific biological activities. Researchers benefit from its reliable performance in solid-phase peptide synthesis (SPPS), enabling the efficient assembly of complex peptide sequences. This compound stands out due to its robust chemical properties and compatibility with various coupling reagents, making it a preferred choice for professionals in the pharmaceutical and biotechnology sectors.

CAS Number
959573-04-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 30 H 33 N º 5
Molecular Weight
487.6
MDL Number
MFCD06410972
PubChem ID
4712552
Appearance
Polvo blanco
Optical Rotation
[α] D = -21 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
959573-04-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C 30 H 33 N º 5
Molecular Weight
487.6
MDL Number
MFCD06410972
PubChem ID
4712552
Appearance
Polvo blanco
Optical Rotation
[α] D = -21 ± 2º (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)-Fmoc-4-amino-5-(4-tert-butoxyphenyl)pentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with the overall peptide structure.
  • Drug Development: Its unique structure can be leveraged in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and specificity.
  • Bioconjugation: The chemical is useful in bioconjugation processes, where it can be attached to biomolecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studies related to neurotransmitter pathways, potentially aiding in the discovery of new treatments for neurological disorders.
  • Material Science: The compound can be utilized in the development of advanced materials, including polymers that require specific functional groups for enhanced properties.

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