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Catalog Number:
29682
CAS Number:
1310680-30-8
(R,S)-Fmoc-3-amino-2-(naphthalen-2-yl)-propionic acid
Purity:
≥ 98% (HPLC)
Documents
$113.87 /25MG
Pack Size Availability Price
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Product Information

(R,S)-Fmoc-3-amino-2-(naphthalen-2-yl)-propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, facilitates the efficient assembly of peptides by providing a stable and easily removable protecting group for the amino functionality. Its unique naphthalene moiety enhances the compound's hydrophobic interactions, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers often leverage this compound in the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where peptide-based drugs are gaining traction.

The compound's ability to improve solubility and stability in various solvents makes it a preferred choice for chemists looking to optimize their synthetic routes. Its application extends to the synthesis of peptide libraries for drug discovery, allowing for high-throughput screening of potential candidates. With its robust performance and adaptability, (R,S)-Fmoc-3-amino-2-(naphthalen-2-yl)-propionic acid stands out as an essential tool for researchers aiming to innovate in peptide chemistry and related fields.

CAS Number
1310680-30-8
Purity
≥ 98% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD18782838
PubChem ID
74892119
Melting Point
172-182 ?C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
CAS Number
1310680-30-8
Purity
≥ 98% (HPLC)
Molecular Formula
C28H23NO4
Molecular Weight
437.49
MDL Number
MFCD18782838
PubChem ID
74892119
Melting Point
172-182 ?C
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Fmoc-3-amino-2-(naphthalen-2-yl)-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of novel drug candidates, particularly in targeting specific biological pathways, enhancing efficacy and reducing side effects compared to traditional compounds.
  • Bioconjugation: The compound can be used to create bioconjugates, linking drugs to targeting moieties, which improves the delivery and effectiveness of therapeutic agents in cancer treatment.
  • Research in Neuroscience: It is employed in studies related to neuropeptides, helping researchers understand neurotransmitter functions and their implications in neurological disorders.
  • Material Science: The compound can be incorporated into polymer matrices to develop advanced materials with specific properties, such as increased strength or enhanced biocompatibility for medical applications.

Citations