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Catalog Number:
05045
CAS Number:
269078-82-2
Fmoc-6-piperazin-1-yl-4(3H-quinazolinone-3-acetic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-Pqa-OH
Documents
$228.24 /100MG
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Product Information

Fmoc-6-piperazin-1-yl-4(3H)-quinazolinone-3-acetic acid is a versatile compound widely utilized in the field of medicinal chemistry and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the synthesis of peptide-based therapeutics. Its structure, characterized by a quinazolinone core, enhances its potential as a bioactive molecule, making it a valuable candidate for various pharmaceutical applications. Researchers have employed this compound in the development of targeted therapies, particularly in oncology and neurology, due to its ability to interact with specific biological targets.

The compound's unique properties, such as its stability and ease of modification, allow for the creation of diverse derivatives tailored for specific therapeutic needs. Its application in peptide synthesis facilitates the production of complex molecules that can lead to innovative treatments. With its growing relevance in drug discovery and development, Fmoc-6-piperazin-1-yl-4(3H)-quinazolinone-3-acetic acid stands out as a crucial tool for researchers aiming to advance therapeutic options in various medical fields.

Synonyms
Fmoc-Pqa-OH
CAS Number
269078-82-2
Purity
≥ 98% (HPLC)
Molecular Formula
C29H26N4O5
Molecular Weight
510.58
MDL Number
MFCD01074698
PubChem ID
2756215
Melting Point
140-167 ºC
Appearance
White to greyish powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-Pqa-OH
CAS Number
269078-82-2
Purity
≥ 98% (HPLC)
Molecular Formula
C29H26N4O5
Molecular Weight
510.58
MDL Number
MFCD01074698
PubChem ID
2756215
Melting Point
140-167 ºC
Appearance
White to greyish 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

Fmoc-6-piperazin-1-yl-4(3H)-quinazolinone-3-acetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific receptors or pathways in disease treatment.
  • Bioconjugation: Researchers use this chemical to create bioconjugates, linking drugs to targeting moieties for enhanced delivery and efficacy in therapeutic applications.
  • Fluorescent Probes: The compound can be utilized in the development of fluorescent probes for imaging studies, aiding in the visualization of biological processes in real-time.
  • Research in Neuroscience: Due to its piperazine moiety, it is explored for its potential effects on neurotransmitter systems, contributing to studies on mental health and neurological disorders.

Citations