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Catalog Number:
05601
CAS Number:
7738-22-9
Boc-L-serine tert-butyl ester
Purity:
≥ 97% (Assay)
Synonym(s):
Boc-L-Ser-OtBu, Boc-L-β-hydroxyalanine tert-butyl ester
Documents
$80.50 /1G
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Product Information

Boc-L-serine tert-butyl ester is a versatile compound widely utilized in peptide synthesis and organic chemistry. This protected amino acid derivative features a tert-butyl ester group, which enhances its stability and solubility, making it an ideal choice for researchers and industry professionals engaged in the development of pharmaceuticals and biologically active compounds. Its unique structure allows for selective deprotection, facilitating the synthesis of complex peptides and proteins.

In addition to its role in peptide synthesis, Boc-L-serine tert-butyl ester is also valuable in the production of various bioactive molecules, including enzyme inhibitors and therapeutic agents. Its application in combinatorial chemistry and drug discovery highlights its significance in advancing medicinal chemistry. Researchers appreciate its ease of use and the efficiency it brings to synthetic pathways, making it a preferred choice for those looking to streamline their processes while achieving high yields.

Synonyms
Boc-L-Ser-OtBu, Boc-L-β-hydroxyalanine tert-butyl ester
CAS Number
7738-22-9
Purity
≥ 97% (Assay)
Molecular Formula
C12H23NO5
Molecular Weight
261.32
MDL Number
MFCD00190832
PubChem ID
13304921
Appearance
White solid/powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Ser-OtBu, Boc-L-β-hydroxyalanine tert-butyl ester
CAS Number
7738-22-9
Purity
≥ 97% (Assay)
Molecular Formula
C12H23NO5
Molecular Weight
261.32
MDL Number
MFCD00190832
PubChem ID
13304921
Appearance
White solid/powder
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 tert-butyl ester is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial for developing complex peptides used in pharmaceuticals.
  • Drug Development: Its application in drug design helps in creating more stable and effective therapeutic agents, particularly in the development of neuroprotective drugs that target specific pathways in the nervous system.
  • Biotechnology: In the field of biotechnology, it is used to enhance the stability of proteins during formulation, which is essential for the production of biopharmaceuticals that require precise activity and shelf-life.
  • Research in Enzyme Activity: Researchers utilize this compound to study enzyme kinetics and mechanisms, providing insights into metabolic pathways that can lead to new therapeutic strategies.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential to improve the stability and efficacy of active ingredients in skincare products, offering enhanced benefits to consumers.

Citations