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Benzenesulfonic acid 2,2,2-trifluoro-1-phenyl-ethyl ester is a complex organic compound with the chemical formula C14H12F3O3S. It is an ester derivative of benzenesulfonic acid, featuring a trifluoroethyl group attached to a phenyl ring. Benzenesulfonic acid 2,2,2-trifluoro-1-phenyl-ethyl ester is characterized by its unique structure, which includes a benzene ring with a sulfonic acid group, a trifluoromethyl group, and an ethyl ester group. It is synthesized by reacting benzenesulfonic acid with 2,2,2-trifluoro-1-phenylethanol in the presence of a suitable catalyst. Due to its specific chemical properties, it has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and specialty chemicals. The compound's stability, reactivity, and solubility can be influenced by the presence of the trifluoromethyl group, which imparts unique characteristics to the molecule.

5042-25-1

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5042-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5042-25-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,4 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5042-25:
(6*5)+(5*0)+(4*4)+(3*2)+(2*2)+(1*5)=61
61 % 10 = 1
So 5042-25-1 is a valid CAS Registry Number.

5042-25-1Downstream Products

5042-25-1Relevant academic research and scientific papers

Catalytic AgF-Initiated Intramolecular 1,3-Sulfonyl Migration of gem-Difluorovinyl Sulfonates to α,α-Difluoro-β-ketosulfones

Chen, Lei,Li, Xiong,Li, Yue,Lian, Zhong,Sun, Haotian,Xiong, Baojian,Xu, Jie

, p. 9263 - 9268 (2020)

A 1,3-sulfonyl migration of difluorovinyl sulfonates initiated by a catalytic amount of silver fluoride is presented. α,α-Difluoro-β-ketosulfones were successfully prepared in excellent yields. This method features high chemoselectivity, good functional group tolerance, high atom economy, and mild, environmentally benign reaction conditions. Furthermore, mechanistic experiments indicate that this migration proceeds in an intermolecular pathway and the corresponding sulfinates are possible intermediates.

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