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(E)-3-phenyl-1-(quinolin-2-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

957785-22-7

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957785-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957785-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,7,8 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 957785-22:
(8*9)+(7*5)+(6*7)+(5*7)+(4*8)+(3*5)+(2*2)+(1*2)=237
237 % 10 = 7
So 957785-22-7 is a valid CAS Registry Number.

957785-22-7Relevant academic research and scientific papers

Synthetic and mechanistic studies on the solvent-dependent copper-catalyzed formation of indolizines and chalcones

Albaladejo, María José,Alonso, Francisco,González-Soria, María José

, p. 3446 - 3456 (2015/06/16)

Copper nanoparticles supported on activated carbon have been found to catalyze the multicomponent synthesis of indolizines from pyridine-2-carbaldehyde derivatives, secondary amines, and terminal alkynes in dichloromethane; in the absence of solvent, howe

Synthesis of indolizines and heterocyclic chalcones catalyzed by supported copper nanoparticles

Albaladejo, Maria Jose,Alonso, Francisco,Yus, Miguel

supporting information, p. 5242 - 5245 (2013/05/21)

Solvent decides: Versatile copper nanoparticles (Cu NPs) on activated carbon have been found to catalyze the multicomponent synthesis of indolizines in dichloromethane and the synthesis of heterocyclic chalcones in the absence of solvent, in both cases, f

Total synthesis of streptonigrone

Chan, Bryan K.,Ciufolini, Marco A.

, p. 8489 - 8495 (2008/02/13)

(Chemical Equation Presented) A total synthesis of streptonigrone, 1, is described, which incorporates a one-step synthesis of substituted pyridones devised in our laboratory. Other aspects of the synthesis that differentiate the present approach from previous ones are the use of a Conrad-Limpach reaction, rather than the customary Friedlaender methodology, to assemble the quinoline segment of 1, and the implementation of an anionic sequence for the functionalization of a key pyridone intermediate.

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