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1,1,2-Trifluoro-2-trifluorovinyl-3-vinyl-cyclobutane is a complex organic compound with the molecular formula C6H3F6. It features a cyclobutane ring, which is a four-carbon cyclic structure, with three vinyl groups (C=CH2) and three fluorine atoms attached to the carbon atoms. The compound has a unique structure where one of the vinyl groups is further substituted with two additional fluorine atoms, making it a trifluorovinyl group. This molecule is of interest in the field of organic chemistry, particularly for its potential applications in the synthesis of fluorinated compounds, which have a wide range of uses in pharmaceuticals, agrochemicals, and materials science. The specific arrangement of fluorine atoms and vinyl groups in 1,1,2-Trifluoro-2-trifluorovinyl-3-vinyl-cyclobutane can influence its reactivity and physical properties, making it a subject of study for chemists looking to understand and exploit the effects of fluorination on molecular behavior.

710-75-8

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710-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 710-75-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 710-75:
(5*7)+(4*1)+(3*0)+(2*7)+(1*5)=58
58 % 10 = 8
So 710-75-8 is a valid CAS Registry Number.

710-75-8Downstream Products

710-75-8Relevant academic research and scientific papers

THE THERMAL CYCLOADDITION OF PERFLUORO-1,3-BUTADIENE WITH BUTA-1,3-DIENE

Weigert, Frank J.

, p. 125 - 131 (2007/10/02)

The major products from the cross-dimerization of butadiene and perfluorobutadiene are a 2+2-cycloadduct and a 2+4-cycloadduct.Perfluorobutadiene is the diene and butadiene is the dienophile.Minor products include the 4+4-cycloadduct, a criss-cross product, and several others containing fluorine on four membered rings.Pyrolysis converts both the 2+2- and the 2+4-adducts to the criss-cross product.Pyrolysis of the 2+2-adduct in the presence of carbon also gives 1,2,3- and 1,2,4-trifluorobenzenes.The fluorine nmr data for C4F6 cycloadducts helps assigning the structures.

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