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3-methyl-5-(methylsulfanyl)-1-phenyl-1H-pyrazolo[4,3-e][1,2,4]triazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

310888-52-9

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310888-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 310888-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,0,8,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 310888-52:
(8*3)+(7*1)+(6*0)+(5*8)+(4*8)+(3*8)+(2*5)+(1*2)=139
139 % 10 = 9
So 310888-52-9 is a valid CAS Registry Number.

310888-52-9Relevant academic research and scientific papers

Transformations of phenylhydrazones of 5-acyl-1,2,4-triazines to pyrazolo[4,3-e][1,2,4]triazines or 4-cyanopyrazole

Mojzych, Mariusz,Rykowski, Andrzej

, p. 1003 - 1007 (2007)

(Chemical Equation Presented) A simple and high yielding preparation of pyrazolo[4,3-e][1,2,4]triazines and 4-cyano-3-methyl-1-phenylpyrazole derivatives from corresponding phenylhydrazones of 5-acyl-1,2,4-triazines by melt under acidic medium and by ther

Direct synthesis of pyrazolo[4,3-e][1,2,4]triazine derivatives from oximes of 5-acyl and 5-formyl-1,2,4-triazines

Mojzych, Mariusz,Rykowski, Andrzej

, p. 191 - 194 (2006)

Deprotection of carbonyl functionality in oximes of 5-acyl and 5-formyl-1,2,4-triazines followed by condensation with hydrazine or substituted hydrazine and subsequent intramolecular ring closure of the resulting hydrazones of 5-acyl and 5-formyl-1,2,4-tr

A new synthesis of pyrazolo[4,3-e][1,2,4]triazines via acid promoted ring closure of the phenylhydrazones of 5-acyl-1,2,4-triazines

Rykowski, Andrzej,Mojzych, Mariusz,Karczmarzyk, Zbigniew

, p. 2175 - 2181 (2007/10/03)

The reaction of various substituted phenylhydrazones of 5-acyl-1,2,4-triazines in the presence of 1.1 equivalent of HCl in boiling ethanol-dioxane mixture has been studied. In all reactions the formation of the corresponding pyrazolo[4,3-e][1,2,4]triazines (3a-r) takes place in good yield. The structures of 3a-r were unequivocally established by spectroscopic methods as well as by X-Ray analysis of selected 5-methyl-3-phenyl-7-(p-tolyl)pyrazolo[4,3-e][1,2,4]triazine (3a).

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