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Catalog Number:
15553
CAS Number:
511272-52-9
Ácido Fmoc-( R -3-amino-3-(2-clorofenil)propiónico
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-β-Phe(2-Cl)-OH, ( R -Fmoc-2-cloro-β-fenilalanina
Documents
$150.00 /1G
Tamaño
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Product Information

Fmoc-(R)-3-amino-3-(2-chlorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound, recognized for its unique structural features, serves as an essential intermediate in the development of bioactive peptides and pharmaceuticals. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection under mild conditions, making it an ideal choice for researchers focused on synthesizing complex peptide sequences. The presence of the 2-chlorophenyl group enhances its biological activity, providing opportunities for the design of novel therapeutic agents targeting various diseases.

In addition to its applications in peptide synthesis, Fmoc-(R)-3-amino-3-(2-chlorophenyl)propionic acid is also valuable in the field of drug discovery, where it can be employed to create libraries of peptide-based compounds for screening against specific biological targets. Its favorable properties, including stability and ease of handling, make it a preferred choice for both academic and industrial laboratories. Researchers can leverage this compound to explore new avenues in drug development, particularly in areas such as cancer therapy and neuropharmacology.

Synonyms
Fmoc-D-β-Phe(2-Cl)-OH, ( R -Fmoc-2-cloro-β-fenilalanina
CAS Number
511272-52-9
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03428034
PubChem ID
22831635
Melting Point
190 - 192 °C
Appearance
White powder
Optical Rotation
[a]D25 = -2.6 ± 1 ° (C=1 in DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-β-Phe(2-Cl)-OH, ( R -Fmoc-2-cloro-β-fenilalanina
CAS Number
511272-52-9
Purity
≥ 98% (HPLC)
Molecular Formula
C24H20ClNO4
Molecular Weight
421.88
MDL Number
MFCD03428034
PubChem ID
22831635
Melting Point
190 - 192 °C
Appearance
White powder
Optical Rotation
[a]D25 = -2.6 ± 1 ° (C=1 in DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(2-chlorophenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules such as proteins and antibodies, which is crucial for creating targeted drug delivery systems.
  • Research in Neuroscience: Its application in neuroscience research aids in studying receptor interactions and signaling pathways, providing insights into neurological disorders and potential treatments.
  • Material Science: The compound's properties allow for its use in creating advanced materials, such as hydrogels, which can be employed in various biomedical applications like tissue engineering.

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