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β,β,β,2,4,5-hexachlorethylbenzene, also known as hexachloroethylbenzene, is a chlorinated organic compound with the chemical formula C8H6Cl6. It is a derivative of ethylbenzene, where three hydrogen atoms on the ethyl group and three hydrogen atoms on the benzene ring are replaced by chlorine atoms. β,β,β,2,4,5-hexachlorethylbenzene is characterized by its high chlorine content, which contributes to its chemical stability and resistance to degradation. Due to its persistence and potential environmental impact, hexachloroethylbenzene is not commonly used in commercial applications and is of interest primarily from a chemical and environmental science perspective. It is important to note that due to its chlorinated nature, it may pose risks to the environment and human health if not handled and disposed of properly.

30359-47-8

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30359-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30359-47-8 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, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30359-47:
(7*3)+(6*0)+(5*3)+(4*5)+(3*9)+(2*4)+(1*7)=98
98 % 10 = 8
So 30359-47-8 is a valid CAS Registry Number.

30359-47-8Downstream Products

30359-47-8Relevant academic research and scientific papers

2,4,5-trisubstituted phenylketo-enols for use as pesticides and herbicides

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, (2008/06/13)

PCT No. PCT/EP96/02606 Sec. 371 Date Dec. 22, 1997 Sec. 102(e) Date Dec. 22, 1997 PCT Filed Jun. 17, 1996 PCT Pub. No. WO97/01535 PCT Pub. Date Jan. 16, 1997The invention relates to new phenyl-substituted cyclic ketoenols of the formula (I) in which Het r

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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