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861015-36-3

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861015-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861015-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,0,1 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 861015-36:
(8*8)+(7*6)+(6*1)+(5*0)+(4*1)+(3*5)+(2*3)+(1*6)=143
143 % 10 = 3
So 861015-36-3 is a valid CAS Registry Number.

861015-36-3Upstream product

861015-36-3Relevant academic research and scientific papers

Synthesis and properties of 1,2-dihydro-4(3H)-quinazolinones

Khachatryan,Belus,Misyurin,Baryshnikova,Kolotaev,Matevosyan

, p. 1044 - 1058 (2017)

We modified the preparative-scale method for the synthesis of 2-aryl 1,2-dihydro-4(3H)-quinazolinone derivatives obtained in high yields by the reaction of new and commercially available aromatic aldehydes with anthranilic acid amides. A series of quinazolinone derivatives possessing anticancer and antiparasitic activities, as well as capable of preventing the progress of neurodegenerative diseases were characterized. There are grounds for clinical trials of these substances in order to select compounds being promising for clinical application.

Novel approach for the synthesis of N-substituted-4-(2-methyl-4-oxo- 4hquinazolin- 3-YL)-butyramides

Amir, Mohammad,Ali, Israr

experimental part, p. 2086 - 2095 (2011/07/31)

A simple and convenient method for the synthesis of N-substituted-4-(2- methyl- 4-oxo-4H-quinazolin-3-yl)-butyramides has been reported. Several aromatic and aliphatic amide derivatives of 4-(2-methyl-4-oxo-4H-quinazolin-3- yl)-butyric acid were prepared

An efficient route to vinyl substituted oxadiazoles and triazoles using phenylselanyl derivatives as precursor

Wang, Yu-Guang,Huang, Xian,Wu, Yu-Zhou

, p. 7866 - 7873 (2008/02/08)

Vinyl substituted oxadiazoles and triazoles were obtained from selenoxide syn-elimination of phenylselanylethyl substituted oxadiazoles and triazoles, which were prepared through hydrazinolysis, acylation, and cyclocondensation reactions of phenylselanyl-

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