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CAS 170449-18-0

:

6,7-Dimethoxy-4-[N-(3-chlorophenyl)amino]quinazoline hydrochloride

Description:
6,7-Dimethoxy-4-[N-(3-chlorophenyl)amino]quinazoline hydrochloride is a synthetic compound belonging to the quinazoline class of heterocyclic compounds. It features a quinazoline core substituted with two methoxy groups at the 6 and 7 positions and an amino group linked to a 3-chlorophenyl moiety at the 4 position. This compound is typically characterized by its solid-state form, often appearing as a hydrochloride salt, which enhances its solubility in aqueous solutions. The presence of the methoxy groups contributes to its lipophilicity, potentially influencing its pharmacokinetic properties. The 3-chlorophenyl substituent may impart specific biological activities, making it of interest in medicinal chemistry, particularly in the development of therapeutic agents targeting various diseases. Its molecular structure suggests potential interactions with biological targets, and it may exhibit properties such as anti-cancer or anti-inflammatory activities, although specific biological effects would require empirical investigation. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C16H14ClN3O2·ClH
InChI:InChI=1S/C16H14ClN3O2.ClH/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-4-10(17)6-11;/h3-9H,1-2H3,(H,18,19,20);1H
InChI key:InChIKey=WDJDYIUSDDVWKB-UHFFFAOYSA-N
SMILES:N(C=1C2=C(C=C(OC)C(OC)=C2)N=CN1)C3=CC(Cl)=CC=C3.Cl
Synonyms:
  • 4-(3-Chloroanilino)-6,7-dimethoxyquinazoline
  • 4-Quinazolinamine, N-(3-chlorophenyl)-6,7-dimethoxy-, hydrochloride (1:1)
  • 4-Quinazolinamine, N-(3-chlorophenyl)-6,7-dimethoxy-, monohydrochloride
  • N-(3-Chlorophenyl)-6,7-dimethoxy-4-quinazolinamine monohydrochloride
  • N-(3-chlorophenyl)-6,7-dimethoxyquinazolin-4-amine
  • N-(3-chlorophenyl)-6,7-dimethoxyquinazolin-4-amine hydrochloride
  • Tyrphostin AG 1478
  • 6,7-Dimethoxy-4-[N-(3-chlorophenyl)amino]quinazoline hydrochloride
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