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Catalog Number:
16874
CAS Number:
145514-62-1
Acide N -Boc-(2 R ,3 R -3-amino-2-hydroxy-3-phénylpropionique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-Ise(3-phényl)-OH, (2 R ,3 S - N - tert -Butoxycarbonyl-3-phénylisosérine
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$93.14 /25 mg
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Product Information

N-Boc-(2R,3R)-3-amino-2-hydroxy-3-phenylpropionic acid is a versatile compound widely utilized in pharmaceutical and biochemical research. 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 development. Its unique structure allows for the introduction of phenyl groups, which can significantly influence the biological activity of the resulting compounds. Researchers often leverage this compound in the design of novel therapeutics, particularly in the fields of neuropharmacology and cancer research, where modifications to amino acids can lead to improved efficacy and selectivity of drug candidates.

The compound's ability to serve as a building block in the synthesis of more complex molecules is a notable advantage, allowing for the exploration of various pharmacophores. Additionally, its favorable properties, such as high purity and consistent performance in reactions, make it a preferred choice among professionals in medicinal chemistry. With its potential applications in drug discovery and development, N-Boc-(2R,3R)-3-amino-2-hydroxy-3-phenylpropionic acid stands out as a valuable tool for researchers aiming to innovate in therapeutic solutions.

Synonyms
Boc-Ise(3-phényl)-OH, (2 R ,3 S - N - tert -Butoxycarbonyl-3-phénylisosérine
CAS Number
145514-62-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C 14 H 195
Molecular Weight
281.3
MDL Number
MFCD02684461
PubChem ID
21254115
Melting Point
82-90 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -39 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-Ise(3-phényl)-OH, (2 R ,3 S - N - tert -Butoxycarbonyl-3-phénylisosérine
CAS Number
145514-62-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C 14 H 195
Molecular Weight
281.3
MDL Number
MFCD02684461
PubChem ID
21254115
Melting Point
82-90 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = -39 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Boc-(2R,3R)-3-amino-2-hydroxy-3-phenylpropionic 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 bioactive compounds and pharmaceuticals.
  • Drug Development: It plays a significant role in medicinal chemistry, where it is used to create novel drug candidates with improved efficacy and reduced side effects.
  • Biotechnology: The compound is employed in the production of biologically active molecules, aiding in the development of therapeutics for various diseases.
  • Research in Neuroscience: Its structural properties make it useful in studies related to neurotransmitter systems, potentially leading to advancements in treatments for neurological disorders.
  • Cosmetic Formulations: The compound is explored in the cosmetic industry for its potential benefits in skin care products, enhancing skin hydration and elasticity.

Citations