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pyrazolo[1,5-a]quinazolin-5(4H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1494669-12-3

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1494669-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1494669-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,9,4,6,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1494669-12:
(9*1)+(8*4)+(7*9)+(6*4)+(5*6)+(4*6)+(3*9)+(2*1)+(1*2)=213
213 % 10 = 3
So 1494669-12-3 is a valid CAS Registry Number.

1494669-12-3Downstream Products

1494669-12-3Relevant academic research and scientific papers

Pyrazolo [1, 5 - a] quinazoline derivatives and their use in pharmaceutical preparations

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Paragraph 0066-0069, (2021/09/08)

The invention relates to a pyrazolo [1, 5 - a] quinazoline derivative as well as a preparation method and application thereof in preparation of medicines. In particular, a compound of formula I is provided. Or a pharmaceutically acceptable salt thereof, o

Water-mediated selective synthesis of pyrazolo[1,5-a ]quinazolin-5(4 H)-ones and [1,2,4]triazolo[1,5-a ]quinazolin-5(4 H)-one via copper-catalyzed cascade reactions

Zhang, Xinying,Gao, Lin,Wang, Zhangxin,Fan, Xuesen

, p. 2426 - 2435 (2015/11/09)

A convenient and sustainable synthesis of pyrazolo[1,5-a]quinazolin-5(4H)-ones and [1,2,4]triazolo[1,5-a]quinazolin-5(4H)-one through copper-catalyzed cascade reactions of 2-bromobenzoates with 1H-pyrazol-5-amines or 1H-1,2,4-triazol-5-amine under ligand-

Pyrazoloquinazolinones and pyrazolopyridopyrimidinones by a sequential N-acylation-SNAr reaction

Gnanasekaran, Krishna Kumar,Prasad Muddala,Bunce, Richard A.

supporting information, p. 1367 - 1369 (2015/03/04)

An efficient synthesis of pyrazolo[1,5-a]quinazolin-5(4H)-ones and pyrazolo[1,5-a]pyrido[3,2-e]pyrimidin-5(4H)-ones is reported from the reaction of 2-haloaroyl chlorides with 5-amino-1H-pyrazoles. The reaction takes advantage of the 1,3-disposition of el

QUINAZOLINE BASED RESPIRATORY SYNCYTIAL VIRUS INHIBITORS

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Page/Page column 52, (2015/05/19)

Compounds of Formula (I), wherein R1, R2, R3, R4 and n are defined herein, are useful as inhibitors of RSV.

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