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

1618654-25-3

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1618654-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1618654-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,8,6,5 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1618654-25:
(9*1)+(8*6)+(7*1)+(6*8)+(5*6)+(4*5)+(3*4)+(2*2)+(1*5)=183
183 % 10 = 3
So 1618654-25-3 is a valid CAS Registry Number.

1618654-25-3Downstream Products

1618654-25-3Relevant academic research and scientific papers

An efficient metal-free synthesis of 2-amino-substituted-4(3H)-quinazolinones

Mirza, Behrooz

, p. 146 - 147 (2015/12/23)

2-Amino-substituted-4(3H)-quinazolinones have been synthesized via an efficient metal-free reaction between 2-aminobenzamide derivatives and carbonimidic dibromides. The reaction proceeds in the presence of K2CO3 affording cyclized products in good to excellent yields.

Synthesis of benzoimidazoquinazolines by cobalt-catalyzed isocyanide insertion-cyclization

Ahmadi, Fereshteh,Bazgir, Ayoob

, p. 61955 - 61958 (2016/07/11)

An efficient and practical protocol for the synthesis of benzoimidazoquinazoline amines in moderate to good yields by the reaction of isocyanides and benzo[d]imidazol-anilines via a cobalt-catalyzed isocyanide insertion cyclization reaction into the two N

One-pot synthesis of 2-amino-4(3H)-quinazolinones via ring-opening of isatoic anhydride and palladium-catalyzed oxidative isocyanide-insertion

Ji, Fei,Lv, Mei-Fang,Yi, Wen-Bin,Cai, Chun

, p. 5766 - 5772 (2014/07/22)

An efficient and practical two-step process has been developed for the synthesis of 2-amino-4(3H)-quinazolinones via ring-opening of isatoic anhydride and palladium-catalyzed oxidative isocyanide-insertion in one pot. This regioselective procedure could construct a wide range of 2-amino-4(3H)- quinazolinones in moderate to excellent yields. Furthermore, the methodology also had distinct advantages of easily accessible starting materials and operational simplicity. the Partner Organisations 2014.

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