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α,α'-Diphenyl-1,4-benzenedimethanol diacetate is a synthetic organic compound with the chemical formula C23H22O4. It is derived from the parent compound α,α'-diphenyl-1,4-benzenedimethanol, which is a chiral molecule with two phenyl rings connected by a central benzene ring, and two hydroxyl groups attached to the carbon atoms at the 1 and 4 positions. The diacetate form is obtained by the esterification of the hydroxyl groups with acetic acid, resulting in the formation of two acetate groups. α,α'-diphenyl-1,4-benzenedimethanol diacetate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the preparation of chiral ligands for asymmetric catalysis. It is characterized by its ability to form stable complexes with metal ions, which can be utilized in the development of new materials with specific properties.

95560-57-9

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95560-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95560-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95560-57:
(7*9)+(6*5)+(5*5)+(4*6)+(3*0)+(2*5)+(1*7)=159
159 % 10 = 9
So 95560-57-9 is a valid CAS Registry Number.

95560-57-9Downstream Products

95560-57-9Relevant academic research and scientific papers

Catalytic Electrophilic Alkylation of p-Quinones through a Redox Chain Reaction

Xu, Xiao-Long,Li, Zhi

, p. 8196 - 8200 (2017)

Allylation and benzylation of p-quinones was achieved through an unusual redox chain reaction. Mechanistic studies suggest that the existence of trace hydroquinone initiates a redox chain reaction that consists of a Lewis acid catalyzed Friedel–Crafts alkylation and a subsequent redox equilibrium that regenerates hydroquinone. The electrophiles could be various allylic and benzylic esters. The addition of Hantzsch ester as an initiator improves the efficiency of the reaction.

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