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Cyclobutane, 3-(difluoromethylene)-1,1-difluoro-2-methylene-, also known as 1,1-difluoro-2-(fluoromethylidene)-3-(fluoromethylene)cyclobutane, is a cyclic organic compound with the molecular formula C5H4F4. It features a cyclobutane ring with two fluoromethylene groups (-CF2-) and one difluoromethylene group (-CF2-CF2-). Cyclobutane, 3-(difluoromethylene)-1,1-difluoro-2-methylene- is of interest in the field of organic chemistry, particularly in the synthesis of fluorinated compounds, which have applications in pharmaceuticals, agrochemicals, and materials science. The presence of fluorine atoms in the molecule can significantly alter its physical and chemical properties, such as reactivity, stability, and lipophilicity, making it a valuable building block for the development of new compounds with specific properties.

2557-72-4

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2557-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2557-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2557-72:
(6*2)+(5*5)+(4*5)+(3*7)+(2*7)+(1*2)=94
94 % 10 = 4
So 2557-72-4 is a valid CAS Registry Number.

2557-72-4Downstream Products

2557-72-4Relevant academic research and scientific papers

Bimolecular kinetic studies with high-temperature gas-phase 19F NMR: Cycloaddition reactions of fluoroolefins

Shtarov,Krusic,Smart,Dolbier Jr.

, p. 9956 - 9962 (2001)

A gas-phase NMR kinetic technique has been used for the first time to obtain accurate measurements of rate constants of some bimolecular, second-order cycloaddition reactions. As a test of the potential use of this technique for the study of second-order reactions, the rate constants and the activation parameters for the cyclodimerization reactions of chlorotrifluoroethylene (CTFE) and tetrafluoroethylene (TFE) were determined in the temperature range 240-340 °C, using a commercial high-temperature NMR probe. Obtaining excellent agreement of the results with published data, the technique was then applied to the reaction of 1,1-difluoroallene with 1,3-butadiene, the results of which indicate that the use of gas-phase NMR for reaction kinetics is particularly valuable when a reagent is available only in small amounts and in cases where there are several competing processes occurring simultaneously. The major processes observed in this reaction are regioselective [2+2] and [2+4] cycloadditions, whose rates and activation parameters were determined [k2=9.3×106 exp(-20.1 kcal mol-1/RT) L/mol-1 S-1 and k3=1.2×106 exp(- 18.4 kcal mol-1/RT) L/mol-1 S-1, respectively] in the temperature range 130-210 °C.

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