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1H-Pyrazole-5-carboxylic acid, 1,3,4-triphenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30020-55-4

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30020-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30020-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,2 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30020-55:
(7*3)+(6*0)+(5*0)+(4*2)+(3*0)+(2*5)+(1*5)=44
44 % 10 = 4
So 30020-55-4 is a valid CAS Registry Number.

30020-55-4Relevant academic research and scientific papers

Synthesis, antimicrobial activity and heterocyclic ring transformation of 5-(pyrazol-5-yl)-1,3,4-oxadiazole-2(3H)-thiones

Shawali,Abdallah,Zayed

, p. 546 - 552 (2007/10/03)

The synthesis and antimicrobial activity of a series of the title thiones were examined. Reaction of such thiones with hydrazonoyl halides, resulted in ring transformation to give 5-acylhydrazono derivatives of 1,3,4-thiadiazoles. The mechanisms of the studied reactions are discussed.

1,3-Dipolar Cycloaddition Reactions of Diphenylnitrilimine with Esters of α,β-Didehydroamino acids

Shawali, Ahmad S.,Fahmi, Abdelgawad A.,Hassaneen, Hamdi M.,Abdallah, Magda A.,Abdelhamid, Hyam A.

, p. 2936 - 2944 (2007/10/02)

Diphenylnitrilimine 5 adds regioselectively to the carbon-carbon double bond of methyl β-aryl-N-benzoyl-α,β-didehydroalaninates 3 to afford the pyrazoline derivatives 6.The regiochemistry of the latter cycloadducts was evidenced chemically by their conver

On the Synthesis of Geminally Functionalized Heterocyclic Aminocarboxylic Acid Esters

Coutouli-Argyropoulou, E.,Thessalonikeos, E.

, p. 1945 - 1948 (2007/10/02)

The title compounds 5 can be easily obtained by two alternative procedures: 1,3-dipolar cycloaddition to benzamidocinnamates 3 prepared by methanolysis of the corresponding oxazolones 1 or methanolysis of the spirooxazolones 4 synthesized by 1,3-dipolar c

1,3-Dipolar Cycloadditions, 89. New Contributions to the Chemistry of Diphenylnitrilimine

Clovis, James S.,Fliege, Werner,Huisgen, Rolf

, p. 3062 - 3070 (2007/10/02)

Methyl propiolate, tetrolate, and phenylpropiolate combine with diphenylnitrilimine (1) to afford regioisomeric cycloadducts; the preferential orientation shifts in the sequence given from the pyrazole-5-carboxylic ester to the 4-carboxylic ester.Correspo

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