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

10204-16-7

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10204-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10204-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10204-16:
(7*1)+(6*0)+(5*2)+(4*0)+(3*4)+(2*1)+(1*6)=37
37 % 10 = 7
So 10204-16-7 is a valid CAS Registry Number.

10204-16-7Downstream Products

10204-16-7Relevant academic research and scientific papers

A facile and selective synthesis of 2-alkylamino-4(3H)-quinazolinones

Liang, Yi,Ding, Ming-Wu,Liu, Zhao-Jie,Liu, Xiao-Peng

, p. 2843 - 2848 (2003)

The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with aliphatic primary amines to give mainly 2-alkylamino-4(3H)-quinazolinones 4 with unusual selectivity.

Solid-phase synthesis of 3H-Quinazolin-4-ones based on an aza Wittig-mediated annulation strategy

Villalgordo, José M.,Obrecht, Daniel,Chucholowsky, Alexander

, p. 1405 - 1407 (1998)

Aza Wittig-mediated annulation provides a highly efficient and straightforward strategy for the parallel synthesis of 3H-quinazolin-4-ones on solid support. The products were recovered in good yields and exhibited excellent purities.

RE[N(SiMe3)2]3-Catalyzed Guanylation/Cyclization of Amino Acid Esters and Carbodiimides

Lu, Chengrong,Gong, Chao,Zhao, Bei,Hu, Lijuan,Yao, Yingming

, p. 1154 - 1159 (2018/02/10)

The example of rare-earth metal-catalyzed guanylation/cyclization of amino acid esters and carbodiimides is well-established, forming 4(3H)-2-alkylaminoquinazolinones in 65-96% yields. The rare-earth metal amides RE[N(TMS)2]3 (RE = Y, Yb, Nd, Sm, La; TMS = SiMe3) showed high activities, and La[N(TMS)2]3 performed best for a wide scope of the substrates.

Molybdenum-mediated synthesis of quinazolin-4(3H)-ones via cyclocarbonylation using microwave irradiation

Roberts, Bryan,Liptrot, David,Luker, Tim,Stocks, Michael J.,Barber, Catherine,Webb, Nicola,Dods, Robert,Martin, Barrie

supporting information; experimental part, p. 3793 - 3796 (2011/08/06)

A new, efficient and practical synthesis of quinazolin-4(3H)-ones is reported via molybdenum-mediated cyclocarbonylation using microwave irradiation. These methods allow access to a wide range of quinazolin-4(3H)-ones in reasonable yields without the need for gaseous carbon monoxide and palladium catalysts. A range of reactions illustrating the wide scope of this chemistry was carried out and all proceeded in reasonable yields.

Synthesis of Some Fused-ring Derivatives from 4(3H)-Quinazolone

Talukdar, P. B.,Sengupta, S. K.,Datta, A. K.

, p. 638 - 640 (2007/10/02)

A few more well-defined mesoionic thiazoloquinazolones have been synthesized and their properties recorded.Attempts to build-up analogous fused-ring mesoionic systems via 2-chloro-3-phenyl-4-quinazolone have not been successful.Several new triazolo

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