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336-14-1

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336-14-1 Usage

General Description

1,2-Dichlorodecafluorocyclohexane, also known by its trade name as "FUMAPEST", is a type of organochlorine compound that was once widely used as a pesticide, specifically for controlling termites in buildings. It is a colorless, viscous liquid that is manufactured through the reaction of cyclohexane with chlorine and fluorine. However, due to its harmful effects on human health and the environment, its use has been heavily restricted and banned in many countries. The chemical has been found to persist in the environment, bioaccumulate in living organisms, and pose a risk to aquatic life, which has led to its classification as a persistent organic pollutant. Studies have also shown that exposure to 1,2-dichlorodecafluorocyclohexane can cause adverse effects on the nervous and reproductive systems in humans.

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 articles and documents

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

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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