336-15-2 Usage
General Description
CHLOROPERFLUOROCYCLOHEXANE is a chemical compound that belongs to the perfluorinated compounds group. It is a chlorinated derivative of perfluorocyclohexane, and it is typically used as a solvent in various industrial processes, such as in the production of plastics, electronics, and pharmaceuticals. CHLOROPERFLUOROCYCLOHEXANE has a high chemical stability, which makes it resistant to heat, chemicals, and other environmental factors. However, it is also known for its potential environmental and health risks, as it is a persistent organic pollutant and has been associated with negative impacts on human health and the environment. As a result, the use and emission of CHLOROPERFLUOROCYCLOHEXANE are regulated in many countries to minimize its potential harmful effects.
Check Digit Verification of cas no
The CAS Registry Mumber 336-15-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 336-15:
(5*3)+(4*3)+(3*6)+(2*1)+(1*5)=52
52 % 10 = 2
So 336-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C6ClF11/c7-1(8)2(9,10)4(13,14)6(17,18)5(15,16)3(1,11)12
336-15-2Relevant articles and documents
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.
