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Catalog Number:
12913
CAS Number:
72648-80-7, 347890-34-0
N-[2-(Boc-amino)ethyl]glycine ethylester hydrochloride
Purity:
≥ 95% (NMR)
Synonym(s):
N-(Boc-aminoethyl)-Gly-OEt·HCl, Ethyl [2-(Boc-amino)ethylamino]acetate hydrochloride
Documents
$77.82 /250MG
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Product Information

N-[2-(Boc-amino)ethyl]glycine ethylester hydrochloride is a versatile compound widely utilized in the fields of biochemistry and pharmaceutical research. This compound, also known as Ethyl 2-[2-[(Boc-amino)ethyl]amino]acetate hydrochloride, features a Boc (tert-butyloxycarbonyl) protecting group that enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug development. Its unique structure allows for easy incorporation into various biochemical pathways, facilitating the design of novel therapeutic agents.

Researchers often leverage N-[2-(Boc-amino)ethyl]glycine ethylester hydrochloride in the synthesis of bioactive peptides and as a building block in the development of enzyme inhibitors. Its ability to serve as a versatile intermediate in organic synthesis opens up possibilities for creating compounds with specific biological activities, thus holding significant potential for advancing drug discovery and development. The compound's favorable properties, such as its stability and ease of handling, make it an essential tool for professionals in medicinal chemistry and related fields.

Synonyms
N-(Boc-aminoethyl)-Gly-OEt·HCl, Ethyl [2-(Boc-amino)ethylamino]acetate hydrochloride
CAS Number
72648-80-7, 347890-34-0
Purity
≥ 95% (NMR)
Molecular Formula
C11H22N2O4·HCl
Molecular Weight
282.76
MDL Number
MFCD01862956
PubChem ID
4319362
Melting Point
116 - 119 °C
Appearance
White to yellow solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-(Boc-aminoethyl)-Gly-OEt·HCl, Ethyl [2-(Boc-amino)ethylamino]acetate hydrochloride
CAS Number
72648-80-7, 347890-34-0
Purity
≥ 95% (NMR)
Molecular Formula
C11H22N2O4·HCl
Molecular Weight
282.76
MDL Number
MFCD01862956
PubChem ID
4319362
Melting Point
116 - 119 °C
Appearance
White to yellow solid
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

N-[2-(Boc-amino)ethyl]glycine ethylester hydrochloride 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 other functional groups.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in developing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of therapeutic agents.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, aiding in the understanding of neurological disorders and the development of potential treatments.
  • Analytical Chemistry: This chemical assists in the development of analytical methods for detecting and quantifying biomolecules, providing researchers with reliable tools for their studies.

Citations