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(2-Chloro-1,1,2-trifluoro-ethyl)-p-tolyl ether is a chemical compound that can be described as an ether derivative, where a p-tolyl group (a methyl group attached to a phenyl ring) is connected to a 2-chloro-1,1,2-trifluoro-ethyl group through an oxygen atom. (2-chloro-1,1,2-trifluoro-ethyl)-p-tolyl ether is characterized by its unique structure, which includes a chlorine atom, three fluorine atoms, and a methyl group attached to different parts of the molecule. It is a colorless liquid with a specific molecular formula and is used in various chemical reactions and processes, particularly in the synthesis of pharmaceuticals and agrochemicals. Due to its specific functional groups, it may exhibit unique reactivity and properties, making it a valuable intermediate in organic chemistry.

350-59-4

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350-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350-59-4 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 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 350-59:
(5*3)+(4*5)+(3*0)+(2*5)+(1*9)=54
54 % 10 = 4
So 350-59-4 is a valid CAS Registry Number.

350-59-4Downstream Products

350-59-4Relevant academic research and scientific papers

Chemistry of Halogenoperfluoroalkanes> Synthesis of Fluorinated Ethers and Thioethers via Radical or Anionic Intermediates

Wakselman, Claude,Tordeux, Marc

, p. 4047 - 4051 (2007/10/02)

Condensation of bromotrifluoromethane with potassium thiophenoxides in DMF is performed under pressure (2-3 atm) in a glass apparatus.Inhibition by nitrobenzene shows that a SRN1 mechanism is involved in the formation of aryl trifluoromethyl sulfides.Dichlorodifluoromethane itself reacts through a similar process to give aryl chlorodifluoromethyl sulfides.Condensation of 1,1,2-trichlorotrifluoroethane with potassium thiophenoxide or phenoxide occurs even in the presence of nitrobenzene.The formation of aryl 2,2-dichloro-1,1,2-trifluoroethyl sulfides or ethers can be explained by a chain carbanionic mechanism.

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