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4H-nonafluoro-cyclohexene is a synthetic chemical compound with the molecular formula C6F10H4. It is a cyclic hydrocarbon with a six-carbon ring structure, where four hydrogen atoms are replaced by fluorine atoms, resulting in a nonafluoro derivative. 4H-nonafluoro-cyclohexene is characterized by its high electronegativity and thermal stability due to the presence of fluorine atoms. It is often used in the production of fluoropolymers and as an intermediate in the synthesis of various fluorinated compounds. The unique properties of 4H-nonafluoro-cyclohexene, such as its resistance to chemical reactions and its low reactivity, make it a valuable component in specialty chemicals and materials science.

1428-38-2

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1428-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1428-38:
(6*1)+(5*4)+(4*2)+(3*8)+(2*3)+(1*8)=72
72 % 10 = 2
So 1428-38-2 is a valid CAS Registry Number.

1428-38-2Relevant academic research and scientific papers

FLUORINATION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Krasilnikov, V. A.,Karelin, A. I.,et al.

, p. 385 - 400 (2007/10/02)

Vanadium pentafluoride reacts with polyfluorinated and polychlorinated olefins, alkadienes, cycloalkenes and cyclodienes in CFCl3 or without a solvent at -25 deg C to 100 deg C, forming products of addition of two fluorine atoms across the C=C bond.

ACTION OF VANADIUM AND ANTIMONY PENTAFLUORIDES ON POLYFLUORINATED DERIVATIVES OF CYCLOHEXADIENE

Avramenko, A. A.,Bardin, V. V.,Furin, G. G.,Karelin, A. I.,Krasil'nikov, V. A.,Tushin, P. P.

, p. 1298 - 1303 (2007/10/02)

Polyfluorinated 1,3- and 1,4-cyclohexadienes are fluorinated by vanadium fluoride at -25 to 25 deg C.The olefinic fragments of perfluoro-1,3- and perfluoro-1,4-cyclohexadienes are close to each other in reactivity.Under the influence of vanadium pentafluoride the fluorine atoms add to 1-R-heptafluoro-1,4-cyclohexadienes preferentially at the multiple bond containing the less electron-withdrawing substituent.At -80 to 20 deg C antimony pentafluoride leads to isomerization of the polyfluorinated derivatives of cyclohexadiene.

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