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CAS 1145671-38-0

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4-Chloro-7-hydroxy-6-quinazolinyl 2,2-dimethylpropanoate

Description:
4-Chloro-7-hydroxy-6-quinazolinyl 2,2-dimethylpropanoate is a chemical compound characterized by its quinazoline core structure, which is a bicyclic compound containing a benzene ring fused to a pyrimidine ring. The presence of a chloro group at the 4-position and a hydroxy group at the 7-position contributes to its unique reactivity and potential biological activity. The ester functional group, derived from 2,2-dimethylpropanoic acid, suggests that this compound may exhibit lipophilic properties, influencing its solubility and permeability in biological systems. This compound may be of interest in medicinal chemistry due to its structural features, which could be associated with various pharmacological activities. Its specific interactions and applications would depend on further studies, including its synthesis, stability, and biological assays. As with many quinazoline derivatives, it may be explored for potential therapeutic uses, particularly in the fields of oncology and neurology, where such compounds have shown promise.
Formula:C13H13ClN2O3
InChI:InChI=1S/C13H13ClN2O3/c1-13(2,3)12(18)19-10-4-7-8(5-9(10)17)15-6-16-11(7)14/h4-6,17H,1-3H3
InChI key:InChIKey=QHCBJLQPMHZHEY-UHFFFAOYSA-N
SMILES:ClC=1C2=C(C=C(O)C(OC(C(C)(C)C)=O)=C2)N=CN1
Synonyms:
  • 4-Chloro-7-hydroxy-6-quinazolinyl 2,2-dimethylpropanoate
  • Propanoic acid, 2,2-dimethyl-, 4-chloro-7-hydroxy-6-quinazolinyl ester
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