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Benzenemethanol, 4-(bromomethyl)-2,3,5,6-tetrafluoro- is a chemical compound with the molecular formula C7H4BrF4O. It is a derivative of benzenemethanol, featuring a bromine atom attached to the methyl group and four fluorine atoms substituting the hydrogen atoms at the 2, 3, 5, and 6 positions on the benzene ring. Benzenemethanol, 4-(bromomethyl)-2,3,5,6-tetrafluoro- is characterized by its unique structure, which provides it with distinct chemical properties and potential applications in various fields, such as pharmaceuticals and agrochemicals. Due to its halogenated nature, it may also be used as an intermediate in the synthesis of other organic compounds.

99705-46-1

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99705-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99705-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,0 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99705-46:
(7*9)+(6*9)+(5*7)+(4*0)+(3*5)+(2*4)+(1*6)=181
181 % 10 = 1
So 99705-46-1 is a valid CAS Registry Number.

99705-46-1Relevant academic research and scientific papers

METHOD FOR PRODUCING 4-METHYL-2,3,5,6-TETRAFLUOROBENZYL ALCOHOL

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Page/Page column 12-13, (2009/12/07)

A process for producing 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol comprising the following steps (A) to (D): Step (A): a step for fluorinating 2,3,5,6-tetrachloroterephthaloyl dichloride, Step (B): a step for reducing the product obtained in step (A), Step (C): a step for chlorinating the product obtained in step (B), Step (D): a step for hydrogenating the product obtained in step (C).

Preparation of one intermediate for pyrethroids

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Page/Page column 4-5, (2008/06/13)

Methods for preparing 2,3,5,6-tetrafluorodimethylolbenzene, an intermediate for the preparation of pyrethroids, are disclosed. A method for preparing 2,3,5,6-tetrafluorodimethylolbenzene includes the reduction of tetrafluoroterephthalate. Various reduction processes are disclosed, which are simple and safe and can afford the product in high yield and purity. Processes for preparing tefluthrin from 2,3,5,6-tetrafluorodimethylolbenzene, by halogenation, hydrogenation, and esterification, are also disclosed.

A CONVENIENT SYNTHESIS OF CERTAIN HYDROXYMETHYL TETRAHALOGENOBENZYL BROMIDES

Costello, Alan T.,Milner, David J.

, p. 219 - 222 (2007/10/02)

Surprisingly, toluene solutions certain tetrahalogenobenzene dimethanols rapidly afford the corresponding hydroxymethyl tetrahalogenobenzyl bromides in about 90percent yield on treatment with hydrobromic acid without the need for continuous removal of the

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