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CAS 162012-67-1

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4-Quinazolinamine, N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitro-

Description:
4-Quinazolinamine, N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitro- is a chemical compound characterized by its quinazolinamine core, which is a bicyclic structure containing both benzene and pyrimidine rings. This compound features several notable substituents, including a chloro and a fluoro group on the phenyl ring, as well as a nitro group and an additional fluoro group on the quinazolinamine structure. These functional groups contribute to its potential biological activity and influence its chemical reactivity. The presence of halogens (chlorine and fluorine) often enhances lipophilicity and can affect the compound's pharmacokinetic properties. The nitro group is known for its electron-withdrawing characteristics, which can impact the compound's reactivity and stability. Overall, this compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural features and potential biological applications. However, specific properties such as solubility, melting point, and biological activity would require empirical data for a comprehensive understanding.
Formula:C14H7ClF2N4O2
InChI:InChI=1/C14H7ClF2N4O2/c15-9-3-7(1-2-10(9)16)20-14-8-4-13(21(22)23)11(17)5-12(8)18-6-19-14/h1-6H,(H,18,19,20)
SMILES:c1cc(c(cc1Nc1c2cc(c(cc2ncn1)F)N(=O)=O)Cl)F
Synonyms:
  • N-(3-chloro-4-fluoro-phenyl)-7-fluoro-6-nitro-quinazolin-4-amine
  • N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitro-4-Quinazolinamine
  • N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitroquinazolin-4-amine
  • N-(3-Chloro-4-fluorophenyl)(7-fluoro-6-nitroquinazolin-4-yl)amine
  • Afatinib int-1 N-(3-Chloro-4-fluorophenyl)-7-fluoro-6-nitro-4-quinazolinamine
  • Afatinib intermediate A
  • )-7-fL
  • N-(3-chloro-4-fluorophenyl)-N-(7-fluoro-6-nitroquinazolin-4-yl)acetaMide
  • uoro-6-nitroquninazoL
  • 4-(3-Chloro-4-fluoroanilino)-7-fluoro-6-nitroquinazoline
  • See more synonyms
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