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2-(4-chlorophenyl)-3-ethylquinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74375-41-0

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74375-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74375-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,7 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74375-41:
(7*7)+(6*4)+(5*3)+(4*7)+(3*5)+(2*4)+(1*1)=140
140 % 10 = 0
So 74375-41-0 is a valid CAS Registry Number.

74375-41-0Downstream Products

74375-41-0Relevant academic research and scientific papers

Rapid assembly of quinazolinone scaffold via copper-catalyzed tandem reaction of 2-bromobenzamides with aldehydes and aqueous ammonia: Application to the synthesis of the alkaloid tryptanthrin

Guo, Shenghai,Li, Yan,Tao, Li,Zhang, Wenwen,Fan, Xuesen

, p. 59289 - 59296 (2015/02/19)

An efficient and practical procedure for the preparation of 2-substituted and 2,3-disubstituted quinazolinones was achieved through copper-catalyzed tandem reaction of 2-bromobenzamides with aldehydes and aqueous ammonia under air. Control experimental results indicated that this tandem reaction is triggered by a copper-catalyzed direct amination of 2-bromobenzamides with aqueous ammonia, followed by cyclocondensation and oxidative aromatization. As an application, this novel methodology provides a concise and practical one-pot route to the synthesis of alkaloid tryptanthrin. This journal is

Synthesis of quinazolinones from alcohols via laccase-mediated tandem oxidation

Heidary, Marjan,Khoobi, Mehdi,Ghasemi, Sabrieh,Habibi, Zohreh,Faramarzi, Mohammad Ali

, p. 1789 - 1794 (2014/06/09)

This paper describes the synthesis of quinazolinones via a tandem reaction using the laccase-mediator system under mild conditions. The procedure involved the laccase-catalyzed oxidation of alcohols to the corresponding aldehydes, followed by cyclocondensation with isatoic anhydride and a number of amines to afford 2,3-dihydroquinazolin-4(1H)-ones, which were further oxidized to quinazolinones in useful yields. The use of an enzyme as the catalyst, O 2 as an environmentally friendly oxidant, and a citrate buffer as the green solvent represents a novel and efficient approach for the one-pot synthesis of quinazolinones.

Efficient one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones from aromatic aldehydes and their one-pot oxidation to quinazolin-4(3H)-ones catalyzed by Bi(NO3)3·5H2O: Investigating the role of the catalyst

Mohammadpoor-Baltork, Iraj,Khosropour, Ahmad R.,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Baghersad, Saeid,Mirjafari, Arsalan

experimental part, p. 944 - 952 (2012/04/23)

An efficient and novel synthesis of 2,3-disubstituted 2,3- dihydroquinazolin-4(1H)-ones via one-pot, three-component reaction of isatoic anhydride, primary amines and aromatic aldehydes catalyzed by Bi(NO 3)3·5H2O under so

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