Product Information
Iodoquinazolin-4(3H)-one is a heterocyclic compound. It is synthesized by the reaction of iodosobenzene with chlorodiacetyl chloride. The protonation of this product leads to the formation of an iodosobenzene diacetate species which can then react with ethyl trifluoroacetate, leading to the formation of 3-amino-2-ethylquinazolin-4(3H)-one. This reaction is driven by the difference in electronegativity between chlorine and oxygen, which results in a partial positive charge on the chlorine atom that can be transferred to another molecule, such as ethyl trifluoroacetate. The frequency of vibration determines how reactive a molecule will be and what type of chemical reactions it will undergo. The orientation of molecules in space determines whether they are reactive or unreactive. Quinazolones are functional groups that are unreactive due to their high
Chemical properties
Technical inquiry about: 3D-ACA54751 3-Amino-2-ethylquinazolin-4(3H)-one
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