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1,5-Cyclooctadiene, 1,4,4,5,8,8-hexafluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92818-41-2

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92818-41-2 Usage

Explanation

The compound consists of 8 carbon atoms, 4 hydrogen atoms, and 6 fluorine atoms.

Explanation

The molecule has a cyclooctane ring with two carbon-carbon double bonds, located at the 1 and 5 positions.

Explanation

The molecule has six fluorine atoms attached to the carbon atoms, which increases its chemical reactivity and alters its properties.

Explanation

The addition of fluorine atoms enhances the reactivity of the molecule, making it more reactive than the parent compound, 1,5-cyclooctadiene.

Explanation

The compound can form stable complexes with transition metal ions, making it useful in organometallic chemistry.

Explanation

Due to its unique structure and reactivity, the compound is utilized in the synthesis of a wide range of organic compounds and materials.

Explanation

The compound serves as a starting material for the synthesis of fluorinated polymers and other chemicals that contain fluorine atoms.

Explanation

The addition of fluorine atoms to the molecule changes its physical properties, such as boiling point, melting point, and solubility, compared to the parent compound.

Explanation

The compound's ability to form stable complexes with transition metal ions contributes to its utility in organometallic chemistry and various applications.

Structure

Eight-membered ring hydrocarbon with two double bonds

Fluorination

Six fluorine atoms added

Chemical Reactivity

Increased due to fluorination

Application

Ligand in organometallic chemistry

Synthesis

Used in the synthesis of various organic compounds and materials

Precursor

In the preparation of fluorinated polymers and other fluorine-containing chemicals

Physical Properties

Altered by fluorination

Stability

Forms stable complexes with transition metal ions

Check Digit Verification of cas no

The CAS Registry Mumber 92818-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,1 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92818-41:
(7*9)+(6*2)+(5*8)+(4*1)+(3*8)+(2*4)+(1*1)=152
152 % 10 = 2
So 92818-41-2 is a valid CAS Registry Number.

92818-41-2Downstream Products

92818-41-2Relevant academic research and scientific papers

2,3,3-Trifluoro-1-cyclobutene and Dimers of 1,1,2-Trifluoro-1,3-butadiene from Tetrafluoroethylene-Vinylsilane Cycloadducts

England, David C.,Weigert, Frank J.,Calabrese, Joseph C.

, p. 4816 - 4819 (1984)

(Tetrafluorocyclobutyl)silanes prepared by thermal cycloaddition of tetrafluoroethylene (TFE) to vinylsilanes were pyrolyzed at 600 deg C to give mixtures containing dimers of 1,1,2-trifluoro-1,3-butadiene.The monomeric diene 1 was undoubtly an intermediate formed by ring opening of initially formed 2,3,3-trifluoro-1-cyclobutene (9).This cyclobutene has been prepared by fluoride ion catalyzed removal of trimethylfluorosilane from (2,2,3,3-tetrafluorocyclobutyl)trimethylsilane (8) at room temperature.One of the dimers of the diene was saturated and was shown by X-raycrystallography to have the tricyclooctane structure (3) corresponding to a previously reported structure for a perfluorobutadiene dimer.The cyclooctadiene 2 presumed to be the precursor to dimer 3 and Diels-Alder dimers (vinylcyclohexenes) 4 and 7 were characterized by 19F NMR analyses of liquid fractions.

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