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1-(2,2,2-trichloroethyl)-2,6-dichlorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30359-34-3

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30359-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30359-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30359-34:
(7*3)+(6*0)+(5*3)+(4*5)+(3*9)+(2*3)+(1*4)=93
93 % 10 = 3
So 30359-34-3 is a valid CAS Registry Number.

30359-34-3Relevant academic research and scientific papers

A phenylacetic acid compound preparation method (by machine translation)

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Paragraph 0099, (2018/03/01)

The invention relates to the field of chemical synthesis, in particular relates to a preparation method of the compound of phenylacetic acid. The present invention provides a preparation method of the compound of phenylacetic acid, the acid compounds of the structural formula states the benzene second grade shown in formula I, the preparation method comprises the following steps: (1) diazo addition reaction: formula II compound containing vinylidene chloride, acid, diazotization reagent, phase transfer catalyst and a copper catalyst in the system of the formula III compound: (2) hydrolysis reaction: the compound of formula III in the presence of acid hydrolysis of formula I compounds. The present invention provides a preparation method of and is simple, easy operation, low cost of raw materials, mild reaction conditions, low risk, does not need to use expensive noble metal catalyst and complex industrial operation means, the product quality is stable, therefore easy achievement of large-scale industrial production. (by machine translation)

Process for the arylation of olefines

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, (2008/06/13)

A process for arylating an olefinic compound by addition of an aryl group to a double bond of said olefinic compound consisting in diazotizing an arylamine in an aqueous acidic solution comprising a lower alkanoic acid to form a solution of an aryldiazonium salt and reacting said aryldiazonium salt solution with an olefinic compound in an organic solvent in the presence of a catalytically effective amount of a copper halide. The amount of alkanoic acid is about 15 to 37% by volume of the total solvents used. The alkanoic acid is preferably acetic acid and the copper halide cuprous chloride.

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