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Benzene, pentafluoro(phenylmethoxy)-, also known as 1-(2,3,4,5,6-pentafluorophenoxy)-2-phenylethane or 2-phenyl-2-(2,3,4,5,6-pentafluorophenoxy)ethane, is an organic compound with the chemical formula C14H9F5O. It is a colorless liquid with a molecular weight of 286.22 g/mol. Benzene, pentafluoro(phenylmethoxy)- is characterized by a benzene ring with five fluorine atoms attached to it, and a phenylmethoxy group (a benzene ring with a methoxy group) attached to the other end. It is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure and properties, it has potential applications in the development of new materials and compounds with specific functionalities.

1644-67-3

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1644-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1644-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1644-67:
(6*1)+(5*6)+(4*4)+(3*4)+(2*6)+(1*7)=83
83 % 10 = 3
So 1644-67-3 is a valid CAS Registry Number.

1644-67-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl pentafluorophenyl ether

1.2 Other means of identification

Product number -
Other names Benzyl-pentafluorphenyl-aether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1644-67-3 SDS

1644-67-3Downstream Products

1644-67-3Relevant academic research and scientific papers

Reactions of polyfluorinated cyclohexadienones with diazoalkanes. Part 1. Formation of cyclopropanes from polyfluorinated cyclohexa-2,4-dienones with diazomethane and phenyldiazomethane

Kovtonyuk, Vladimir N.,Kobrina, Ljubov S.,Gatilov, Yurij V.,Bagryanskaya, Irina Yu.,Froehlich, Roland,Haufe, Guenter

, p. 1929 - 1933 (2007/10/03)

The reaction of 6-chloro-2,3,4,5,6-pentafluorocyclohexa-2,4-dienone (1) with diazomethane gives a mixture of two diastereoisomers of 6-chloro-3a,4,5,6,7a-pentafluoro-3,3a,6,7a-tetrahydrospiro[indazole-7,2′-o xirane] 2a and 2b. In contrast phenyldiazomethane reacts with polyfluorinated cyclohexa-2,4-dienones 1, 9, and 10 in acetonitrile to form the fluorinated 7-phenylbicyclo[4.1.0]hept-4-en-2-ones 4a,b, 11a,b, and 12a,b as the main products. This reaction shows a remarkable dependence on the polarity of the solvent. While a complex mixture of products was formed in pentane, the reaction in acetonitrile proceeds with high stereoselectivity giving only the two endo-isomers.

Electron Affinities of Fluorinated Phenoxy Radicals

Hernandez-Gil, N.,Wentworth, W. E.,Chen, E. C. M.

, p. 6181 - 6185 (2007/10/02)

The electron-capture coefficients for five fluorophenoxy phenyl ethers have been determined by using "short" pulse intervals.The temperature dependence of the electron-capture coeficients can be used to determine the electron affinities of the molecules a

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