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"4-{1-[4-(benzoyloxy)phenyl]-1-methylethyl}phenyl benzoate" is a complex organic compound with the molecular formula C28H24O4. It is a derivative of benzoic acid, featuring a benzoyloxy group attached to a phenyl ring, which is further connected to another phenyl ring through a methylene bridge. This molecule is characterized by its ester linkage and the presence of a bulky, multi-ring structure. It is likely to be found in the realm of pharmaceuticals or as an intermediate in the synthesis of more complex organic molecules, given its intricate structure. The compound's specific properties, such as solubility, reactivity, and potential applications, would depend on its chemical environment and the context in which it is used.

2297-14-5

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2297-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2297-14-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2297-14:
(6*2)+(5*2)+(4*9)+(3*7)+(2*1)+(1*4)=85
85 % 10 = 5
So 2297-14-5 is a valid CAS Registry Number.

2297-14-5Downstream Products

2297-14-5Relevant academic research and scientific papers

Scandium trifluoromethanesulfonate as an extremely active Lewis acid catalyst in acylation of alcohols with acid anhydrides and mixed anhydrides

Ishihara, Kazuaki,Kubota, Manabu,Kurihara, Hideki,Yamamoto, Hisashi

, p. 4560 - 4567 (2007/10/03)

Scandium trifluoromethanesulfonate (triflate), which is commercially available, is a practical and useful Lewis acid catalyst for acylation of alcohols with acid anhydrides or the esterification of alcohols by carboxylic acids in the presence of p-nitrobenzoic anhydrides. The remarkably high catalytic activity of scandium triflate can be used for assisting the acylation by acid anhydrides of not only primary alcohols but also sterically-hindered secondary or tertiary alcohols. The method presented is especially effective for selective macrolactonization of ω-hydroxy carboxylic acids.

Process for making esters

-

, (2008/06/13)

Carboxylic acid esters are produced by the reaction of a carboxylic acid halide with a carbonate ester in the presence of an initiator. The reaction of a dicarboxylic acid dihalide and a bis(alkyl carbonate) ester produces a polymeric polyester.

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