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1-Fluoro-1,2,3,4,5,6-hexabromocyclohexane is a complex organic compound with the chemical formula C6Br6F. It is a brominated and fluorinated derivative of cyclohexane, featuring six bromine atoms and one fluorine atom attached to the cyclohexane ring. 1-Fluoro-1,2,3,4,5,6-hexabromocyclohexane is characterized by its high molecular weight and significant halogen content, which contributes to its unique chemical and physical properties. Due to its structure, it exhibits a high degree of thermal stability and resistance to decomposition, which can be advantageous in certain industrial applications. However, the presence of multiple halogen atoms also raises concerns about its environmental impact and potential health risks, as halogenated compounds can be persistent and bioaccumulative in the environment. As a result, the use and handling of such chemicals are often subject to strict regulations to minimize their release into the environment.

359-90-0

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359-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359-90-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 359-90:
(5*3)+(4*5)+(3*9)+(2*9)+(1*0)=80
80 % 10 = 0
So 359-90-0 is a valid CAS Registry Number.

359-90-0Upstream product

359-90-0Downstream Products

359-90-0Relevant academic research and scientific papers

PHOTOCHEMICAL BROMINATION OF ARENES. 2. FLUOROBENZENE DERIVATIVES (1)

Bolton, Roger,Owen, Elaine S. E.

, p. 393 - 406 (2007/10/02)

Photochemically induced reaction of fluorobenzene and a range of polyfluorobenzenes, both in an excess of the arene and with fluorotrichloromethane as solvent, gave isolable adducts only with fluorobenzene, the isomeric difluorobenzenes, and in very small yield with 1,3,5-trifluorobenzene.These adducts were identified by combustion analysis, mass spectrometry, and n.m.r. techniques (1H, 13C, 19F).In every case, the expected substitution products accompanied these adducts, and in the more fully fluorinated benzene derivatives substitution was the only process observed.Fluorotrichloromethane encouraged the formation of adducts, but the concurrent formation of substantial amounts of substitution products suggested that adducts are not the necessary precursors of the substitution products, in contrast with other systems.

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