Date published: 2025-9-5

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Quinazoline (CAS 253-82-7)

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Alternate Names:
1,3-Benzodiazine; Benzopyrimidine
CAS Number:
253-82-7
Purity:
98%
Molecular Weight:
130.15
Molecular Formula:
C8H6N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Quinazoline is a nitrogen-containing heterocyclic compound characterized by a fused structure of benzene and pyrimidine rings, making it a versatile scaffold in chemical synthesis and research exploration outside of therapeutic contexts. The unique bicyclic architecture of quinazoline allows it to function effectively in various chemical interactions, particularly in binding with DNA and enzymes, where its planar nature facilitates intercalative or groove-binding modes of action. In research environments, quinazoline′s core structure is frequently modified to create a multitude of derivatives, each designed to study different biochemical and pharmacological properties. These modifications often aim to explore the impact of different substituents on the molecule′s electronic properties, solubility, and stability, providing insights into the relationship between molecular structure and activity. This makes quinazoline a fundamental compound in the study of heterocyclic chemistry and in the development of novel compounds for industrial and biochemical applications. By enabling detailed investigations into molecular design and interaction mechanisms, quinazoline and its derivatives play a crucial role in advancing the field of organic chemistry and enhancing our understanding of complex molecular systems.


Quinazoline (CAS 253-82-7) References

  1. Quinazoline and benzimidazole MCH-1R antagonists.  |  Arienzo, R., et al. 2007. Bioorg Med Chem Lett. 17: 1403-7. PMID: 17178222
  2. Synthesis and in vitro antitumor activity of substituted quinazoline and quinoxaline derivatives: search for anticancer agent.  |  Noolvi, MN., et al. 2011. Eur J Med Chem. 46: 2327-46. PMID: 21458891
  3. Sulfur and selenium derivatives of quinazoline and pyrido[2,3-d]pyrimidine: synthesis and study of their potential cytotoxic activity in vitro.  |  Moreno, E., et al. 2012. Eur J Med Chem. 47: 283-98. PMID: 22104973
  4. Synthesis of Novel Derivatives of Quinazoline Schiff base Compound Promotes Epithelial Wound Healing.  |  Bagheri, E., et al. 2018. Curr Pharm Des. 24: 1395-1404. PMID: 29384057
  5. The role of quinazoline in ameliorating intervertebral disc degeneration by inhibiting oxidative stress and anti-inflammation via NF-κB/MAPKs signaling pathway.  |  Chen, ZB., et al. 2020. Eur Rev Med Pharmacol Sci. 24: 2077-2086. PMID: 32141577
  6. Discrimination between Protonation Isomers of Quinazoline by Ion Mobility and UV-Photodissociation Action Spectroscopy.  |  Marlton, SJP., et al. 2020. J Phys Chem Lett. 11: 4226-4231. PMID: 32368922
  7. Aromaticity indices, electronic structural properties, and fuzzy atomic space investigations of naphthalene and its aza-derivatives.  |  Edim, MM., et al. 2021. Heliyon. 7: e06138. PMID: 33553781
  8. The Antibacterial Activity of Quinazoline and Quinazolinone Hybrids.  |  Li, Z., et al. 2022. Curr Top Med Chem. 22: 1035-1044. PMID: 35255796
  9. Quantum Mechanical Study of the Competitive Hydration between Protonated Quinazoline and Li+, Na+, and Ca2+ Ions  |  Sawunyama, P., & Bailey, G. W. 2001. The Journal of Physical Chemistry A. 105(42): 9717-9724.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Quinazoline, 1 g

sc-250828
1 g
$42.00