336-13-0 Usage
Uses
Used in Industrial Applications:
1-BROMOUNDECAFLUOROCYCLOHEXANE is used as a solvent, refrigerant, and propellant in various industries due to its unique properties that include high chemical stability and resistance to heat and chemicals.
Used in Polymer and Plastics Production:
1-BROMOUNDECAFLUOROCYCLOHEXANE is used as a component in the production of polymers and plastics, where its high fluorination contributes to the desired material characteristics.
Used in Environmental and Health Regulations:
Due to its status as a persistent organic pollutant with the potential to bioaccumulate in the environment and pose risks to human health and the ecosystem, 1-BROMOUNDECAFLUOROCYCLOHEXANE is subject to regulatory measures and restrictions in many countries to mitigate its environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 336-13-0 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 336-13:
(5*3)+(4*3)+(3*6)+(2*1)+(1*3)=50
50 % 10 = 0
So 336-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C6BrF11/c7-1(8)2(9,10)4(13,14)6(17,18)5(15,16)3(1,11)12
336-13-0Relevant 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.
