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Benzoic acid, 3,5-bis(3-hydroxy-1-propynyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

422569-47-9

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422569-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 422569-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,2,5,6 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 422569-47:
(8*4)+(7*2)+(6*2)+(5*5)+(4*6)+(3*9)+(2*4)+(1*7)=149
149 % 10 = 9
So 422569-47-9 is a valid CAS Registry Number.

422569-47-9Relevant academic research and scientific papers

An improved sonogashira coupling procedure for the construction of rigid aromatic multifunctional monomers bearing 1,3-substituted acetylenic units

Davidson, Louise,Freebairn, Keith W.,Russell, Andrew T.,Trivedi, Harish S.,Hayes, Wayne

, p. 251 - 254 (2002)

The efficient synthesis of rigid multifunctional vinylic monomers 1 and 2 from 3,5-dibromobenzene derivatives and propargyl alcohol via the Sonogashira reaction is reported. For example, a series of 3,5-bis(3-hydroxyprop-1-ynl)benzoate ester derivatives have been prepared efficiently using an improved palladium catalyst system. Subsequent hydrolysis and reaction with 4-vinylaniline afforded a new monomer 2 for use in functional macroporous polymer systems. In addition, Sonogashira and Wittig methodologies have been optimised in order to construct successfully an alternative rigid monomer 1 from 3,5-dibromobenzaldehyde.

Synthesis and evaluation of a solid supported molecular tweezer type receptor for cholesterol

Davidson, Louise,Blencowe, Anton,Drew, Michael G. B.,Freebairn, Keith W.,Hayes, Wayne

, p. 758 - 766 (2007/10/03)

A new macroporous stationary phase bearing 'tweezer' receptors that exhibit specificity for cholesterol has been constructed from rigid multifunctional vinylic monomers derived from 3,5-dibromobenzoic acid, propargyl alcohol and cholesterol. The synthesis

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