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6-amino-4-(3-chlorophenyl)-3-phenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

401643-95-6

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401643-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401643-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,6,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 401643-95:
(8*4)+(7*0)+(6*1)+(5*6)+(4*4)+(3*3)+(2*9)+(1*5)=116
116 % 10 = 6
So 401643-95-6 is a valid CAS Registry Number.

401643-95-6Downstream Products

401643-95-6Relevant academic research and scientific papers

An efficient and green synthesis of 6-amino-3-phenyl-4-aryl-1,4- dihydropyrano [2,3-c]pyrazole-5-carbonitrile derivatives under ultrasound irradiation in aqueous medium

Zou, Yi,Hu, Yu,Liu, Hai,Shi, Da-Qing

, p. 1174 - 1179 (2013/10/21)

A facile and eco-friendly approach for the synthesis of 6-amino-3-phenyl-4-aryl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile derivatives via four-component reaction of hydrazine, ethyl 3-oxo-3- phenylpropanoate, aldehydes, and malononitrile is described. The reaction is performed in water, without using any catalyst, and under ultrasound irradiation. The developed sonochemical-assisted multi-component reaction provides an improved and accelerated conversion when compared with conventional procedure.

Pyrazolones as building blocks in heterocyclic synthesis: Synthesis of new pyrazolopyran, pyrazolopyridazine and pyrazole derivatives of expected antifungicidal activity

Ramiz, Mahmoud M. M.,Abdel Hafiz, Ibrahim S.,Abdel Reheim, Mohamed A. M.,Gaber, Hatem M.

experimental part, p. 72 - 80 (2012/06/30)

A series of new pyrazolone and pyrazole derivatives with expected antifungicidal activity have been prepared through the reactions 3-phenyl-1-H-pyrazol-5(4H)-one (3) and 4-(dimethylaminomethylene)-3-phenyl-1H- pyrazol-5(4H)-one (5) with a variety of electrophilic reagents and nucleophilic reagents. The newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral studies.

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