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3-Benzyloxyquinazolin-4(3H)-one is a chemical compound belonging to the quinazolinone class, characterized by a quinazoline core structure with a benzyloxy group attached at the 3-position. 3-benzyloxyquinazolin-4(3H)-one is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various quinazoline-based drugs. It exhibits a molecular formula of C15H12N2O2 and a molecular weight of 248.27 g/mol. The presence of the benzyloxy group endows 3-benzyloxyquinazolin-4(3H)-one with unique chemical and biological properties, making it a valuable intermediate in the development of new therapeutic agents targeting a range of diseases.

4797-76-6

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4797-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4797-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4797-76:
(6*4)+(5*7)+(4*9)+(3*7)+(2*7)+(1*6)=136
136 % 10 = 6
So 4797-76-6 is a valid CAS Registry Number.

4797-76-6Downstream Products

4797-76-6Relevant academic research and scientific papers

Method for efficiently preparing quinazolone compounds

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Page/Page column 6, (2017/04/20)

The invention discloses a method for efficiently preparing quinazolone compounds. According to the method, 3-oxyquinazoline and methyl aromatic hydrocarbons are used as substrate, a copper salt is used as a catalyst, 5.5M tert-butyl hydroperoxide in decane is used as an oxidizer, tetrabutyl ammonium iodide and sodium iodide are used as additives, dichloromethane is used as a solvent, and the reaction is carried out at 50-100 DEG C to obtain the quinazolone compounds, wherein the reaction general formula is (1). The 3-oxyquinazoline and methyl aromatic hydrocarbons are subjected to one-step reaction to directly synthesize the quinazolone compounds, and thus, the method has the advantages of direct and simple reaction, low substrate limitation and high reaction efficiency and has wide potential application value.

APPLICATION OF QUARTERNARY PHOSPHONIUM SALTS IN ALKYLATION AND ACYLATION OF N-HYDROXYLACTAMS

Grochowski, Edward,,Boleslawska, Teresa

, p. 615 - 621 (2007/10/02)

Reactions of N-hydroxylactams with alcohols and carboxylic acids in presence of triphenylphosphine and diethyl azodicarboxylate have been described.Contrary to corresponding acyclic amides (hydroxamic acids), cyclic compounds form under these conditions O

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