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Chemical Structure| 1769-24-0 Chemical Structure| 1769-24-0
Chemical Structure| 1769-24-0

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2-Methylquinazolin-4-ol is an efficient competitive poly(ADP-ribose) synthetase inhibitor with a Ki value of 1.1 μM, and it also inhibits mammalian aspartate aminotransferase (ATCase) with an IC50 value of 0.20 mM.

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Product Details of 2-Methylquinazolin-4-ol

CAS No. :1769-24-0
Formula : C9H8N2O
M.W : 160.17
SMILES Code : OC1=C2C=CC=CC2=NC(C)=N1
MDL No. :MFCD05270928

Safety of 2-Methylquinazolin-4-ol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 2-Methylquinazolin-4-ol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1769-24-0 ]

[ 1769-24-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1769-24-0 ]
  • [ 51997-51-4 ]
  • 3-(3-((9H-carbazol-4-yl)oxy)-2-hydroxypropyl)-2-methylquinazolin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% With tetra-(n-butyl)ammonium iodide; potassium carbonate; In acetonitrile; at 80℃; for 36h;Inert atmosphere; General procedure: A mixture of 2-methyl quinazolin-4(3H)-one 3a (150 mg,0.937 mmol), <strong>[51997-51-4]4-(oxiran-2-ylmethoxy)-9H-carbazole</strong> (8, 222 mg,0.937 mmol), potassium carbonate (258 mg, 1.875 mmol) and tetrabutylammonium iodide (5 mg, 0.014 mol) were heated in acetonitrile (15 mL) at 80 C for 36 h under nitrogen atmosphere. The reaction mass was extracted with ethyl acetate, separated and the organic layer was dried over sodium sulfate and concentrated. The crude product was purified by column chromatography over silica gel (65:35, ethyl acetate/hexane) to give following compounds.
 

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