336-15-2 Usage
Description
CHLOROPERFLUOROCYCLOHEXANE is a perfluorinated chemical compound that is a chlorinated derivative of perfluorocyclohexane. It is characterized by its high chemical stability, making it resistant to heat, chemicals, and other environmental factors. However, it is also recognized as a persistent organic pollutant with potential environmental and health risks.
Uses
Used in Industrial Processes:
CHLOROPERFLUOROCYCLOHEXANE is used as a solvent in various industrial applications, including the production of plastics, electronics, and pharmaceuticals. Its high chemical stability and resistance to environmental factors make it a valuable component in these industries.
Used in Manufacturing:
In the manufacturing sector, CHLOROPERFLUOROCYCLOHEXANE is utilized as a solvent to facilitate the production of various products. Its properties allow for efficient manufacturing processes and the creation of high-quality end products.
Regulation and Environmental Considerations:
Due to its status as a persistent organic pollutant and its potential negative impacts on human health and the environment, the use and emission of CHLOROPERFLUOROCYCLOHEXANE are regulated in many countries. This aims to minimize its harmful effects and promote safer alternatives in industrial applications.
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.
