Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
04016
CAS Number:
2766-43-0
Éster metílico de Boc-L-serina
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Boc-L-Ser-OMe, Éster metílico de Boc-L-β-hidroxialanina, Éster metílico del ácido (S)-Boc-2-amino-3-hidroxipropiónico
Documents
$18.53 /5G
Tamaño
Request Bulk Quote
Product Information

Boc-L-serine methyl ester is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Its unique structure allows for selective reactions, facilitating the formation of complex peptides and proteins. Researchers often leverage Boc-L-serine methyl ester in the development of therapeutics, particularly in the design of bioactive peptides that can target specific biological pathways.

In addition to its role in peptide synthesis, Boc-L-serine methyl ester serves as a valuable building block in the production of chiral intermediates and can be employed in the synthesis of various pharmaceuticals. Its favorable properties, such as high purity and ease of handling, make it a preferred choice for both academic and industrial laboratories. With its broad applicability and essential role in advancing peptide chemistry, Boc-L-serine methyl ester continues to be a crucial component in the toolkit of researchers and industry professionals alike.

Synonyms
Boc-L-Ser-OMe, Éster metílico de Boc-L-β-hidroxialanina, Éster metílico del ácido (S)-Boc-2-amino-3-hidroxipropiónico
CAS Number
2766-43-0
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C9H17Nº5
Molecular Weight
219.24
MDL Number
MFCD00191869
PubChem ID
495564
Appearance
Líquido amarillento claro
Optical Rotation
[a] D 20 = -20 ± 3 º (C= 1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Ser-OMe, Éster metílico de Boc-L-β-hidroxialanina, Éster metílico del ácido (S)-Boc-2-amino-3-hidroxipropiónico
CAS Number
2766-43-0
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C9H17Nº5
Molecular Weight
219.24
MDL Number
MFCD00191869
PubChem ID
495564
Appearance
Líquido amarillento claro
Optical Rotation
[a] D 20 = -20 ± 3 º (C= 1 en MeOH)
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 methyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly for those requiring protected amino acids. Its stability and ease of handling make it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, Boc-L-serine methyl ester is used to create bioactive compounds. Its ability to modify biological activity is crucial in developing new therapeutics.
  • Bioconjugation: This chemical is employed in bioconjugation processes, where it helps in attaching biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities.
  • Protein Engineering: Researchers utilize it in the modification of proteins, allowing for the introduction of specific functionalities that can improve protein stability and activity.
  • Analytical Chemistry: Boc-L-serine methyl ester is also used in analytical applications, such as chromatography, where it aids in the separation and identification of complex mixtures.

Citas