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Catalog Number:
11432
CAS Number:
145514-62-1
Boc-(2R,3 S -3-fenilisoserina
Purity:
≥ 99 % (HPLC)
Synonym(s):
(2 R ,3 S -3-(Boc-amino)-2-hidroxi-3-fenil-propanoico
Documents
$127.79 /100 mg
Tamaño
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Product Information

Intermedio para la síntesis de taxol.

Synonyms
(2 R ,3 S -3-(Boc-amino)-2-hidroxi-3-fenil-propanoico
CAS Number
145514-62-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 19 N.º 5
Molecular Weight
281.31
MDL Number
MFCD02259481
PubChem ID
21254115
Melting Point
129-134 ºC
Appearance
Polvo blanquecino
Optical Rotation
[a] D 20 = + 50 ± 2 º (C=1 en NaOH 1N)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(2 R ,3 S -3-(Boc-amino)-2-hidroxi-3-fenil-propanoico
CAS Number
145514-62-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 14 H 19 N.º 5
Molecular Weight
281.31
MDL Number
MFCD02259481
PubChem ID
21254115
Melting Point
129-134 ºC
Appearance
Polvo blanquecino
Optical Rotation
[a] D 20 = + 50 ± 2 º (C=1 en NaOH 1N)
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

Boc-(2R,3S)-3-phenylisoserine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of biologically active compounds and pharmaceuticals.
  • Drug Development: Its unique structure allows for the design of novel drugs targeting specific biological pathways, making it essential in medicinal chemistry.
  • Biotechnology: Used in the production of enzyme inhibitors and other biotechnological applications, it enhances the efficacy of therapeutic agents.
  • Research in Neuroscience: The compound is instrumental in studying neuroactive peptides, contributing to advancements in understanding neurological disorders.
  • Cosmetic Formulations: Its properties can be leveraged in skincare products for potential anti-aging effects, appealing to the cosmetic industry.

Citas