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1,3-Diphenylpropan-2-yl benzoate is a chemical compound with the molecular formula C22H22O2. It is a derivative of 1,3-diphenylpropan-2-ol, where the hydroxyl group is esterified with benzoic acid. This organic ester is characterized by its aromatic structure, featuring two phenyl rings attached to a propane chain, with a benzoate group at the end. It is a colorless to pale yellow solid and is soluble in organic solvents. 1,3-diphenylpropan-2-yl benzoate is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical structure, which can be further modified to create a range of different molecules. Its properties, such as its reactivity and stability, make it a valuable intermediate in organic chemistry.

5565-59-3

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5565-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5565-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5565-59:
(6*5)+(5*5)+(4*6)+(3*5)+(2*5)+(1*9)=113
113 % 10 = 3
So 5565-59-3 is a valid CAS Registry Number.

5565-59-3Downstream Products

5565-59-3Relevant academic research and scientific papers

Base-catalyzed selective esterification of alcohols with unactivated esters

Zhang, Chunyan,Zhang, Guoying,Luo, Shizhong,Wang, Chunfu,Li, Huiping

supporting information, p. 8467 - 8471 (2018/12/01)

A practical and efficient base-catalyzed esterification has been developed for the facile synthesis of a broad range of esters from simple alcohols with unactivated tert-butyl esters. This protocol could be conducted at mild conditions, providing esters in high to excellent yields with good functional tolerance. Mechanistic studies provided evidence of an exchange of the tert-butyl alkoxide metal with the alcohol, producing a new alkoxide to participate in the transesterification reaction.

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