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Catalog Number:
05600
CAS Number:
59524-02-6
Boc-L-serine benzyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Ser-OBzl, Boc-L-β-hydroxyalanine benzyl ester, (S-Boc-2-amino-3-hydroxypropionic acid benzyl ester
Documents
$18.53 /1G
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Product Information

Boc-L-serine benzyl ester is a versatile compound widely utilized in the synthesis of peptides and other bioactive molecules. This protected amino acid derivative features a benzyl ester group that enhances its solubility and stability, making it an ideal choice for researchers engaged in peptide synthesis and drug development. Its unique structure allows for selective deprotection, facilitating the incorporation of L-serine into various peptide sequences, which is crucial in the development of therapeutics and biologically active compounds.

In addition to its applications in peptide chemistry, Boc-L-serine benzyl ester serves as a valuable building block in the production of pharmaceuticals and agrochemicals. Its ability to undergo various chemical transformations while maintaining the integrity of the serine side chain makes it a preferred choice for chemists looking to create complex molecular architectures. With its favorable properties and broad applicability, Boc-L-serine benzyl ester stands out as an essential tool for professionals in medicinal chemistry and related fields.

Synonyms
Boc-L-Ser-OBzl, Boc-L-β-hydroxyalanine benzyl ester, (S-Boc-2-amino-3-hydroxypropionic acid benzyl ester
CAS Number
59524-02-6
Purity
≥ 99% (HPLC)
Molecular Formula
C15H21NO5
Molecular Weight
295.34
MDL Number
MFCD00076983
PubChem ID
12953535
Melting Point
65 - 75 ºC
Appearance
White powder
Optical Rotation
[a]20D = -16 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 8°C
General Information
Synonyms
Boc-L-Ser-OBzl, Boc-L-β-hydroxyalanine benzyl ester, (S-Boc-2-amino-3-hydroxypropionic acid benzyl ester
CAS Number
59524-02-6
Purity
≥ 99% (HPLC)
Molecular Formula
C15H21NO5
Molecular Weight
295.34
MDL Number
MFCD00076983
PubChem ID
12953535
Melting Point
65 - 75 ºC
Appearance
White powder
Optical Rotation
[a]20D = -16 ± 2 º (C=1 in EtOH)
Conditions
Store at 0 - 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-L-serine benzyl ester 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 pharmaceuticals and biologically active compounds. Its protective group allows for selective reactions, enhancing efficiency in complex synthesis pathways.
  • Drug Development: In medicinal chemistry, it is used to create prodrugs that improve the solubility and bioavailability of therapeutic agents. This application is crucial in developing effective treatments with better patient outcomes.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This is particularly valuable in creating targeted drug delivery systems and diagnostic tools.
  • Research in Enzyme Inhibition: It is used in studies aimed at understanding enzyme mechanisms and developing inhibitors. This application is important in drug discovery, particularly for diseases where enzyme activity is a target.
  • Protein Modification: Boc-L-serine benzyl ester is utilized in modifying proteins to study their function and interactions. This application is essential in fields like biotechnology and molecular biology, where understanding protein behavior is key.

Citations