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Catalog Number:
12780
CAS Number:
254101-11-6
Boc-O-benzyl-L-β-homothreonine
Purity:
≥ 95% (NMR)
Synonym(s):
Boc-L-β-HomoThr(Bzl)-OH, (3R,4R-4-Benzyloxy-3-(Boc-amino)pentanoic acid
Documents
$79.22 /100MG
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Product Information

Boc-O-benzyl-L-b-homothreonine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a unique Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. Its structural characteristics allow for selective reactions, facilitating the development of novel therapeutic agents, particularly in the fields of drug discovery and development.

In addition to its applications in peptide synthesis, Boc-O-benzyl-L-b-homothreonine serves as a crucial building block in the design of bioactive compounds, including those targeting specific biological pathways. Its ability to mimic natural amino acids while providing enhanced stability makes it a preferred choice for researchers aiming to create more effective and targeted treatments. The compound's versatility and effectiveness in various synthetic routes underscore its importance in both academic and industrial settings, paving the way for innovative advancements in medicinal chemistry.

Synonyms
Boc-L-β-HomoThr(Bzl)-OH, (3R,4R-4-Benzyloxy-3-(Boc-amino)pentanoic acid
CAS Number
254101-11-6
Purity
≥ 95% (NMR)
Molecular Formula
C17H25NO5
Molecular Weight
323.39
MDL Number
MFCD01862935
PubChem ID
4393168
Appearance
Syrupy Oil
Optical Rotation
[a]D20 = -1.0 ± 2º (C=1 in CHCl3)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-HomoThr(Bzl)-OH, (3R,4R-4-Benzyloxy-3-(Boc-amino)pentanoic acid
CAS Number
254101-11-6
Purity
≥ 95% (NMR)
Molecular Formula
C17H25NO5
Molecular Weight
323.39
MDL Number
MFCD01862935
PubChem ID
4393168
Appearance
Syrupy Oil
Optical Rotation
[a]D20 = -1.0 ± 2º (C=1 in CHCl3)
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-O-benzyl-L-b-homothreonine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting other functional groups, enhancing the efficiency of creating complex peptides.
  • Drug Development: It is used in the development of pharmaceutical compounds, particularly in creating peptide-based drugs that target specific biological pathways, providing a tailored approach to treatment.
  • Biotechnology: This chemical plays a crucial role in the production of biologically active peptides, which are essential in various biotechnological applications, including enzyme production and vaccine development.
  • Research in Neuroscience: The compound is utilized in studies related to neuropeptides, helping researchers understand their role in brain function and potential therapeutic targets for neurological disorders.
  • Analytical Chemistry: It is employed in analytical methods for characterizing peptide structures, aiding in the quality control of peptide-based products and ensuring their efficacy and safety.

Citations