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CAS 4765-56-4

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2-(Phenylmethyl)-4(3H)-quinazolinone

Description:
2-(Phenylmethyl)-4(3H)-quinazolinone, with the CAS number 4765-56-4, is an organic compound that belongs to the quinazolinone class of heterocyclic compounds. It features a quinazolinone core, which is characterized by a fused bicyclic structure containing both a benzene and a pyrimidine ring. This compound typically exhibits a white to off-white crystalline appearance and is known for its potential biological activities, including antimicrobial and anticancer properties. The presence of the phenylmethyl group enhances its lipophilicity, which may influence its pharmacokinetic properties. In terms of solubility, quinazolinones generally show variable solubility in organic solvents, and their reactivity can be attributed to the functional groups present in the structure. The compound's synthesis often involves cyclization reactions, and it may serve as a precursor or intermediate in the development of pharmaceuticals. As with many quinazolinones, it is important to handle this compound with care, adhering to safety protocols due to potential toxicity and reactivity.
Formula:C15H12N2O
InChI:InChI=1S/C15H12N2O/c18-15-12-8-4-5-9-13(12)16-14(17-15)10-11-6-2-1-3-7-11/h1-9H,10H2,(H,16,17,18)
InChI key:InChIKey=ZDUVLDCZFKNYHH-UHFFFAOYSA-N
SMILES:O=C1C=2C(NC(CC3=CC=CC=C3)=N1)=CC=CC2
Synonyms:
  • 2-(Phenylmethyl)-4(3H)-quinazolinone
  • 2-Benzyl-1H-quinazolin-4-one
  • 2-Benzyl-4-quinazolinone
  • 2-Benzylquinazolin-4(3H)-one
  • 4(1H)-quinazolinone, 2-(phenylmethyl)-
  • 4(3H)-Quinazolinone, 2-benzyl-
  • 4(3H)-quinazolinone, 2-(phenylmethyl)-
  • Glycophymine
  • Glycosminine
  • N-Demethylarborine
  • 2-Benzylquinazolin-4(1H)-one
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