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4-chloro-4'-hydroxybenzophenone potassium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22197-31-5

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22197-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22197-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22197-31:
(7*2)+(6*2)+(5*1)+(4*9)+(3*7)+(2*3)+(1*1)=95
95 % 10 = 5
So 22197-31-5 is a valid CAS Registry Number.

22197-31-5Downstream Products

22197-31-5Relevant academic research and scientific papers

Polyether ketone, its monomer and its phenolate

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Page/Page column 9, (2009/10/06)

A process for the preparation of an alkali metal salt of 4-chloro-4'-hydroxy benzophenone comprising of the steps of (a) preparing purified 4-chloro-4'-hydroxy benzophenone by a process comprising distilling under reduced pressure a liquid containing 4-ch

Polymerisation and Related Reactions involving Nucleophilic Aromatic Substitution. Part 1. The Rates of Reaction of Substituted 4-Halogenobenzophenones with the Potassium Salts of Substituted 4-Hydroxybenzophenones

Ridd, John H.,Yousaf, Taher I.,Rose, John B.

, p. 1729 - 1734 (2007/10/02)

The rate of displacement of fluorine from 4'-X,4-fluorobenzophenones by the potassium salts of 4'-X,4-hydroxybenzophenones (X = CF3, Cl, F, H, OPh, and OMe) has been studied at 175-225 deg C in diphenyl sulphone as solvent.Comparison with the corresponding rate of displacement of chlorine indicates that the reaction is a bimolecular nucleophilic aromatic substitution.The reaction obeys the Hammett equation using normal ? values for substitution in both the substrate (ρ 1.19) and the phenolate (ρ -0.53).There is also a marked salt effect on the reaction rate and this has been included with the substituent constants in a general equation for the calculation of rate coefficients.The effect of an O- substituent is more marked than would have been expected from the previous range of ? values ascribed to this substituent.

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