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Catalog Number:
01379
CAS Number:
3262-72-4
Boc-L-sérine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Boc-L-Ser-OH, Boc-L-β-hydroxyalanine, Acide (S)-Boc-2-amino-3-hydroxypropionique
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Product Information

Matière de départ pour la synthèse de divers acides aminés a via la b-lactone.

Synonyms
Boc-L-Ser-OH, Boc-L-β-hydroxyalanine, Acide (S)-Boc-2-amino-3-hydroxypropionique
CAS Number
3262-72-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 8 H 15 NON 5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -8,5 ± 2 º (C = 3 dans H 2 O)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-Ser-OH, Boc-L-β-hydroxyalanine, Acide (S)-Boc-2-amino-3-hydroxypropionique
CAS Number
3262-72-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 8 H 15 NON 5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -8,5 ± 2 º (C = 3 dans H 2 O)
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-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: It serves as a protected amino acid in the synthesis of peptides, allowing for the selective introduction of serine residues without unwanted reactions.
  • Drug Development: Researchers use Boc-L-serine to create biologically active compounds, particularly in the development of pharmaceuticals targeting neurological disorders.
  • Bioconjugation: This compound is valuable in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Protein Engineering: In protein engineering, Boc-L-serine is used to modify protein structures, improving their stability and functionality for various applications in biotechnology.
  • Research in Enzyme Activity: It plays a role in studying enzyme mechanisms, particularly those involving serine residues, providing insights into metabolic pathways and enzyme functions.

Citations