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1,2-Dichlorodecafluorocyclohexane, commercially known as "FUMAPEST", is an organochlorine compound that was once extensively utilized as a pesticide for termite control in buildings. It is a colorless, viscous liquid synthesized through the reaction of cyclohexane with chlorine and fluorine. However, due to its persistence in the environment, bioaccumulation in living organisms, and harmful effects on human health and aquatic life, its use has been heavily restricted and banned in many countries. Classified as a persistent organic pollutant, exposure to 1,2-dichlorodecafluorocyclohexane can lead to adverse effects on the nervous and reproductive systems in humans.

336-14-1

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336-14-1 Usage

Uses

Used in Pesticide Industry:
1,2-Dichlorodecafluorocyclohexane was used as a termiticide for controlling termites in buildings due to its effectiveness in eliminating these pests. Its application was based on its ability to penetrate wood and other building materials, providing long-lasting protection against termite infestations.
However, due to the harmful effects of 1,2-dichlorodecafluorocyclohexane on human health and the environment, its use has been heavily restricted and banned in many countries. Alternative, safer, and more environmentally friendly pest control methods have been developed and adopted in place of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 336-14-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 336-14:
(5*3)+(4*3)+(3*6)+(2*1)+(1*4)=51
51 % 10 = 1
So 336-14-1 is a valid CAS Registry Number.
InChI:InChI=1/C6Cl2F10/c7-1(9)2(8,10)4(13,14)6(17,18)5(15,16)3(1,11)12

336-14-1Relevant academic research and scientific papers

THE PREPARATION AND PROPERTIES OF PERFLUORO-n-HEPTYLBROMINE(V) TETRAFLUORIDE

Habibi, M. H.,Sams, L. C.

, p. 287 - 294 (1982)

Reactions of n-C7F15Br with elemental fluorine at 0 deg C have produced perfluoro-n-heptylbromine(V) tetrafluoride (n-C7F15BrF4).This derivative of BrF5 was characterized by IR, 19F-NMR, mass spectroscopy and elemental alnalysis.The reactions of n-C7F15Br

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.

REACTION OF POLYFLUORINATED CYCLOALKANES WITH VANADIUM, ANTIMONY, AND NIOBIUM PENTAFLUORIDES

Bardin, V. V.,Avramenko, A. A.,Petrov, V. A.,Krasil'nikov, V. A.,Karelin, A. I.,et al

, p. 536 - 540 (2007/10/02)

Polyfluorinated cycloalkanes are fluorinated by vanadium pentafluoride at 25-60 deg C.Conjugation between the C=C bond of the cycloalkene and the aromatic ring facilitates the reaction, whereas the reactivity of the unconjugated olefin fragment is lower than or is equal to that of the aromatic ring.The antimony pentafluoride fluorinates polyhalogenocyclohexenes at 150 deg C, while niobium pentafluoride does not exhibit fluorinating characteristics under these conditions.

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