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Catalog Number:
05030
CAS Number:
204322-92-9
Fmoc-3-(2-aminoethyl)-1-carboxymethylquinazoline-2,4-dione
Purity:
≥ 97%
Synonym(s):
Fmoc-Acq-OH
Documents
$106.96 /100MG
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Product Information

Fmoc-3-(2-aminoethyl)-1-carboxymethylquinazoline-2,4-dione is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure includes a quinazoline core, known for its biological activity, making it an attractive candidate for drug development and research applications. Researchers appreciate its stability and ease of handling, which facilitate efficient synthesis processes.

In practical applications, Fmoc-3-(2-aminoethyl)-1-carboxymethylquinazoline-2,4-dione is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to enhance solubility and improve the pharmacokinetic properties of peptides makes it a preferred choice among chemists and pharmaceutical researchers. Additionally, the compound's unique properties allow for the exploration of novel drug candidates targeting various diseases, including cancer and neurological disorders.

Synonyms
Fmoc-Acq-OH
CAS Number
204322-92-9
Purity
≥ 97%
Molecular Formula
C27H23N3O6
Molecular Weight
485.5
MDL Number
MFCD00673791
PubChem ID
2756207
Appearance
White solid
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-Acq-OH
CAS Number
204322-92-9
Purity
≥ 97%
Molecular Formula
C27H23N3O6
Molecular Weight
485.5
MDL Number
MFCD00673791
PubChem ID
2756207
Appearance
White 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

Fmoc-3-(2-aminoethyl)-1-carboxymethylquinazoline-2,4-dione is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective formation of peptide bonds without unwanted side reactions.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The chemical is used to create bioconjugates, linking biomolecules to drugs or imaging agents, enhancing the efficacy of targeted therapies in cancer treatment.
  • Fluorescent Probes: It can be incorporated into fluorescent probes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.
  • Research in Neuroscience: This compound is being explored for its potential applications in neuroscience, particularly in studying receptor interactions and signaling pathways.

Citations