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Catalog Number:
15557
CAS Number:
500770-74-1
Acide boc-( S -3-amino-3-(3-chlorophényl)propionique)
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-β-Phe(3-Cl)-OH, ( S -Boc-3-chloro-β-phénylalanine
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$72.31 /250 mg
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Product Information

Boc-(S)-3-amino-3-(3-chlorophenyl)propionic acid is a valuable compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug formulation. Its unique structure allows for the selective modification of peptides, facilitating the development of novel therapeutics, particularly in the fields of oncology and neurology. Researchers appreciate its ability to serve as a building block in the synthesis of bioactive compounds, enabling the exploration of new drug candidates with improved efficacy and reduced side effects.

In addition to its role in peptide synthesis, Boc-(S)-3-amino-3-(3-chlorophenyl)propionic acid has shown potential in various applications, including the development of enzyme inhibitors and receptor modulators. Its specific properties, such as chirality and functional group versatility, make it a preferred choice for chemists aiming to create compounds with targeted biological activity. By incorporating this compound into their research, professionals can enhance their ability to innovate and discover new therapeutic agents.

Synonyms
Boc-L-β-Phe(3-Cl)-OH, ( S -Boc-3-chloro-β-phénylalanine
CAS Number
500770-74-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 14 H 18 ClNO 4
Molecular Weight
299.75
MDL Number
MFCD03427921
PubChem ID
4404164
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -38 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Boc-L-β-Phe(3-Cl)-OH, ( S -Boc-3-chloro-β-phénylalanine
CAS Number
500770-74-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 14 H 18 ClNO 4
Molecular Weight
299.75
MDL Number
MFCD03427921
PubChem ID
4404164
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -38 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(S)-3-amino-3-(3-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 the development of pharmaceuticals targeting specific biological pathways.
  • Drug Development: It plays a crucial role in the design of new drugs, especially in the field of neuropharmacology, where modifications to amino acids can enhance drug efficacy and selectivity.
  • Biochemical Research: Researchers use this compound to study protein interactions and enzyme functions, helping to elucidate mechanisms of action in various biological systems.
  • Material Science: Its properties make it suitable for creating specialized materials, including polymers that can be used in drug delivery systems or as scaffolds in tissue engineering.
  • Analytical Chemistry: The compound is utilized in analytical methods to quantify amino acids in biological samples, providing insights into metabolic processes and disease states.

Citations