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1,2-Diphenyl-1,4-dihydroquinazolin-4-one is a chemical compound with the molecular formula C20H16N2O. It is a derivative of quinazolinone, a heterocyclic compound with a fused benzene ring and a pyrimidine ring. This specific compound features two phenyl groups attached to the first and second carbon atoms of the quinazolinone core, and it exists in a dihydro form, indicating the presence of a double bond that has been reduced to a single bond. It is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various bioactive molecules. The compound is also of interest due to its potential as a precursor in the development of new pharmaceuticals and as a ligand in coordination chemistry.

1236-29-9

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1236-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1236-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236-29:
(6*1)+(5*2)+(4*3)+(3*6)+(2*2)+(1*9)=59
59 % 10 = 9
So 1236-29-9 is a valid CAS Registry Number.

1236-29-9Downstream Products

1236-29-9Relevant academic research and scientific papers

Palladium-Catalyzed Carbonylative Reactions of 1-Bromo-2-fluorobenzenes with Various Nucleophiles: Effective Combination of Carbonylation and Nucleophilic Substitution

Chen, Jianbin,Natte, Kishore,Neumann, Helfried,Wu, Xiao-Feng

, p. 16107 - 16110 (2014)

systematic study on the carbonylative transformation of 1-bromo-2-fluorobenzenes with various nucleophiles has been performed. Different types of double nucleophiles, such as N-N, N-C, O-C, and N-S, can be effectively applied as coupling partners. The cor

Synthesis of quinazolin-4(1 H)-ones via amination and annulation of amidines and benzamides

Hu, Fangpeng,Cui, Xinfeng,Ban, Zihui,Lu, Guoqiang,Luo, Nan,Huang, Guosheng

, p. 2356 - 2360 (2019/03/06)

Quinazolinones have broad applications in the biological, pharmaceutical and material fields. Studies on the synthesis of these compounds are therefore widely conducted. Herein, a novel and highly efficient copper-mediated tandem C(sp2)-H amination and annulation of benzamides and amidines for the synthesis of quinazolin-4(1H)-ones is proposed. This synthetic route can be useful for the construction of quinazolin-4(1H)-one frameworks.

1,2,3-Benzotriazin-4-ones and Related Systems. Part 6. Thermal and Photolytic Decomposition of 3-Arylideneamino-, 3-Imidoyl-, and 3-Heteroaryl-1,2,3-benzotriazin-4-ones

Paterson, Thomas McC.,Smalley, Robert K.,Suschitzky, Hans,Barker, Alan J.

, p. 633 - 638 (2007/10/02)

Thermal decomposition of 3-arylideneamino- and 3-imidoyl-1,2,3-benzotriazin-4-ones in solution gives 2-arylquinazolin-4-ones and 1,2-diaryl-1,4-dihydroquinazolin-4-ones, respectively.In the latter decompositions phenanthridones are also formed in minor but substantial (20percent) yield.Possible mechanisms to account for these products are discussed.Photolysis of the 3-arylideneamino-derivatives in methanol provides a useful synthesis of aldehyde o-(methoxycarbonyl)phenylhydrazones. 3-(α-Pyridyl)- and 3-thiazol-2-yl-1,2,3-benzotriazin-4-one undergo thermal decomposition to pyridoquinazolin-11-one and thiazoloquinazolin-5-one, respectively.

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