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1-Chloro-3-(1,1-dichloro-2,2,2-trifluoro-ethyl)-benzene is a complex organic compound with the molecular formula C8H4Cl3F3. It is a halogenated aromatic compound, characterized by the presence of chlorine and fluorine atoms attached to a benzene ring. The molecule consists of a benzene ring with one chlorine atom at the 1st position and a 1,1-dichloro-2,2,2-trifluoroethyl group attached at the 3rd position. 1-chloro-3-(1,1-dichloro-2,2,2-trifluoro-ethyl)-benzene is known for its unique chemical properties, such as its high reactivity and stability, which make it useful in various chemical synthesis processes and as an intermediate in the production of pharmaceuticals and agrochemicals. Due to its complex structure and potential applications, it is an important compound in the field of organic chemistry.

309-12-6

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309-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 309-12-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 309-12:
(5*3)+(4*0)+(3*9)+(2*1)+(1*2)=46
46 % 10 = 6
So 309-12-6 is a valid CAS Registry Number.

309-12-6Downstream Products

309-12-6Relevant academic research and scientific papers

MECHANISMS OF FREE-RADICAL REACTIONS. XIII. MECHANISM AND SELECTIVITY OF THE FREE-RADICAL HALOGENATION OF ALKYL AROMATIC HYDROCARBONS WITH FLUOROALKYL SUBSTITUENTS

Dneprovskii, A. S.,Eliseenkov, E. V.,Mil'tsov, S. A.

, p. 317 - 324 (2007/10/02)

The free-radical chlorination and bromination of 1-fluoro-2-arylethanes and 1,1,1-trifluoro-2-arylethanes was studied by the method of competing reactions.In all cases a good correalation between log krel and the Brown ?+ constants was observed.The variation of the selectivity in the transition from one reaction series to the other indicates that two independent factors which determine the reactivity (the change in the dissociation energy of the C-H bond and the polar effect of the substituents) have a simultaneous effect.

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