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Catalog Number:
01379
CAS Number:
3262-72-4
Boc-L-serina
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Boc-L-Ser-OH, Boc-L-β-Hidroxialanina, Ácido (S)-Boc-2-amino-3-hidroxipropiónico
Documents
$18.50 /5G
Tamaño
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Product Information

Material de partida para la síntesis de varios a-aminoácidos a través de la b-lactona.

Synonyms
Boc-L-Ser-OH, Boc-L-β-Hidroxialanina, Ácido (S)-Boc-2-amino-3-hidroxipropiónico
CAS Number
3262-72-4
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C8H15NO5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -8,5 ± 2 º (C=3 en H 2 O)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Ser-OH, Boc-L-β-Hidroxialanina, Ácido (S)-Boc-2-amino-3-hidroxipropiónico
CAS Number
3262-72-4
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C8H15NO5
Molecular Weight
205.22
MDL Number
MFCD00037243
PubChem ID
294907
Melting Point
90 - 94 °C
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -8,5 ± 2 º (C=3 en H 2 O)
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

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.

Citas