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CarbaMic acid, N-[(1S)-1-[3,4-dihydro-5-Methyl-3-(2-Methylphenyl)-4-oxo-2-quinazolinyl]ethyl]-, 1,1-diMethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

936024-96-3

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936024-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936024-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,0,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 936024-96:
(8*9)+(7*3)+(6*6)+(5*0)+(4*2)+(3*4)+(2*9)+(1*6)=173
173 % 10 = 3
So 936024-96-3 is a valid CAS Registry Number.

936024-96-3Downstream Products

936024-96-3Relevant academic research and scientific papers

COMPOUNDS, COMPOSITIONALS, AND METHODS FOR TREATING T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA

-

, (2019/02/15)

In an aspect, the disclosure provides for compounds (II), compositions, and methods of administering the compounds and compositions to a patient in need thereof. In another aspect, the disclosure relates to compounds and compositions for treating cancer,

A novel highly stereoselective synthesis of 2,3-disubstituted 3H-quinazoline-4-one derivatives

Zhichkin, Paul,Kesicki, Edward,Treiberg, Jennifer,Bourdon, Lisa,Ronsheim, Matthew,Ooi, Hua Chee,White, Stephen,Judkins, Angela,Fairfax, David

, p. 1415 - 1418 (2007/10/03)

Figure presented An efficient three-step synthesis of chiral 3H-quinazoline-4-one derivatives from commercial materials is disclosed. The Mumm reaction of imidoyl chloride with α-amino acids followed by reductive cyclization affords enantiomerically pure (ee >93%) quinazoline-4-ones in good overall yield. A comparison with existing approaches indicates that this method is superior for hindered substrates.

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