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2-Amino-4-(4-chlorophenyl)-4H-pyrano[3,2-h]quinoline-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132546-97-5

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132546-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132546-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,4 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132546-97:
(8*1)+(7*3)+(6*2)+(5*5)+(4*4)+(3*6)+(2*9)+(1*7)=125
125 % 10 = 5
So 132546-97-5 is a valid CAS Registry Number.

132546-97-5Relevant academic research and scientific papers

Halogenated 2-amino-4H-pyrano[3,2-h]quinoline-3-carbonitriles as antitumor agents and structure–activity relationships of the 4-, 6-, and 9-positions

Fouda, Ahmed M.

, p. 302 - 313 (2017/01/28)

A series of halogenated 2-amino-4-aryl-4H-pyrano[3,2-h]quinoline-3-carbonitrile derivatives were prepared via interaction of 8-hydroxyquinoline, 5-chloro-8-hydroxyquinoline, and 8-hydroxy-2-methylquinoline with various α-cyanocinnamonitriles. The assignme

InCl3 promoted synthesis of pyrano[3,2-h]quinolines via microwave irradiation

Kumar, Gopal Senthil,Zeller, Matthias,Frasso, Michael A.,Prasad, Karnam Jayarampillai Rajendra

supporting information, p. 926 - 930 (2015/05/13)

An efficient and economical method has been developed for the synthesis of pyrano[3,2-h]quinolines via an indium trichloride-catalyzed one-pot three-component reaction of 8-hydroxyquinoline with aromatic aldehydes and malononitrile/ethyl cyanoacetate unde

Microwave assisted synthesis of 2-amino-4-(aryl)-4H-pyrano [3,2-H] quinoline-3-carbonitriles in polyethylene glycol and their antibacterial activity

Sarasija,Sudershan,Ashok,Shivaraj

, p. 377 - 380 (2019/01/21)

A series of 2-amino-4-(aryl)-4H-pyrano [3,2-h] quinoline-3-carbonitriles have been synthesized by microwave assisted multicomponent one-pot cyclocondensation reaction of aromatic aldehydes, malononitrile and 8-hydroxy quinoline in PEG-400. All these compo

Synthesis, antitumor activity, and structure-activity relationship of some 4H-pyrano[3,2-h]quinoline and 7H-pyrimido[4′,5′:6,5]pyrano[3,2-h] quinoline derivatives

El-Agrody, Ahmed M.,Abd-Rabboh, Hisham S. M.,Al-Ghamdi, Abdullah M.

, p. 1339 - 1355 (2013/04/10)

Several 4H-pyrano[3,2-h]quinoline (3a-d, 4a, 7a,b, 9a-c, 10a,b, 11a,b, and 13a-c) and 7H-pyrimido[4′,5′:6,5]pyrano[3,2-h]quinoline derivatives (8a-c) were obtained by treatment of 8-hydroxyquinoline (1a) and 8-hydroxy-2-methylquinoline (1b) with α-cyano-p

Synthesis of certain novel 4H-pyrano[3,2-h]quinoline derivatives

El-Agrody, Ahmed M.,Al-Ghamdi, Abdullah M.

experimental part, p. 134 - 146 (2012/02/04)

Treatment of 8-hydroxyquinoline 1a and 8-hydroxy-2-methylquinoline 1b with α-cyano-pchloro/bromocinnamonitriles 2a,b provided 4H-pyrano[3,2-h] quinoline-3-carbonitrile derivatives 3a-d, while treatment of (E) 2-(4-chlorostyryl)-8-hydroxyquinoline 7 with α

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