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Triphenyl-acetic acid 2,2,2-trifluoro-ethyl ester is a complex organic compound with the chemical formula C23H17F3O2. It is an ester derivative of triphenylacetic acid, where the hydroxyl group is replaced by a 2,2,2-trifluoroethyl group. Triphenyl-acetic acid 2,2,2-trifluoro-ethyl ester is characterized by its three phenyl rings attached to the central acetic acid chain and the presence of three fluorine atoms in the ethyl ester group. It is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various drugs and intermediates. The compound's unique structure, with fluorine atoms providing increased lipophilicity and metabolic stability, makes it an interesting candidate for the development of new therapeutic agents.

80054-85-9

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80054-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80054-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,5 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80054-85:
(7*8)+(6*0)+(5*0)+(4*5)+(3*4)+(2*8)+(1*5)=109
109 % 10 = 9
So 80054-85-9 is a valid CAS Registry Number.

80054-85-9Downstream Products

80054-85-9Relevant academic research and scientific papers

Acid-Catalyzed Reaction of 2,2,2-Trifluorodiazoethane for Analysis of Functional Groups by 19F Nuclear Magnetic Resonance Spectrometry

Koller, K. L.,Dorn, H. C.

, p. 529 - 533 (2007/10/02)

The acid-catalyzed reactions of trifluorodiazoethane with alcohols, phenols, thiols, and carboxylic acids are reported.The yield data for these trifluoroethyl derivatives suggest a simple, and in many cases, quantitative method for introduction of a fluorine tagging group.The 19F chemical shifts indicate that most functional groups (e.g., phenols, alcohols, etc.) have fairly well resolved chemical shifts regions.In addition, paramagnetic shift reagents have been utilized to selectively differentiate carboxylic acids from other active hydrogen functional groups.

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