🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
31662
CAS Number:
204200-06-6
Boc-Pro-y(CH2NH)-Gly-OH
Purity:
≥ 99.0% (HPLC)
Documents
$72.31 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-Pro-?(CH2NH)-Gly-OH 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 the selective protection of amino groups, facilitating the formation of complex peptides and proteins. Researchers often leverage this compound in the development of therapeutic peptides, where precise control over amino acid sequences is crucial for efficacy and safety.

In addition to its role in peptide synthesis, Boc-Pro-?(CH2NH)-Gly-OH is also valuable in the study of enzyme interactions and drug design. Its ability to mimic natural amino acids while providing a stable framework for modifications makes it a preferred choice for medicinal chemists. The compound's favorable properties, including its compatibility with various coupling reagents and its ease of deprotection, streamline the synthesis process, ultimately leading to more efficient research and development timelines.

CAS Number
204200-06-6
Purity
≥ 99.0% (HPLC)
Molecular Formula
C12H22N2O4
Molecular Weight
258.32
MDL Number
MFCD00273439
PubChem ID
4712527
Appearance
White powder
Optical Rotation
[a]D20 = - 26 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
204200-06-6
Purity
≥ 99.0% (HPLC)
Molecular Formula
C12H22N2O4
Molecular Weight
258.32
MDL Number
MFCD00273439
PubChem ID
4712527
Appearance
White powder
Optical Rotation
[a]D20 = - 26 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-Pro-?(CH2NH)-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential for drug development and biological research.
  • Drug Development: Its unique structure allows for the creation of novel pharmaceutical compounds, particularly in the field of targeted therapies.
  • Bioconjugation: It is employed in bioconjugation processes, linking biomolecules for applications in diagnostics and therapeutics.
  • Research in Neuroscience: The compound is used to study neuropeptides, contributing to advancements in understanding neurological disorders.
  • Custom Synthesis: It is favored in custom synthesis projects due to its versatility and effectiveness in producing specific molecular configurations.

Citations