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α-Methoxy-α-trifluoromethylphenylselenoacetic acid α-trifluoromethylbenzyl ester is a complex organic compound with the molecular formula C16H13F6O3Se. It is a derivative of selenoacetic acid, featuring a trifluoromethylbenzyl ester group and a methoxy group attached to the phenyl ring. α-Methoxy-α-trifluormethylphenylessigsaeure-α-trifluormethylbenzylester is characterized by its unique structure, which includes a selenium atom bonded to a carbonyl group, a trifluoromethyl group, and a benzyl group. It is synthesized for various applications in organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals, due to its potential reactivity and the influence of the selenium and fluorine atoms on its chemical properties. The compound's specific reactivity and stability make it a subject of interest in the field of organoselenium chemistry.

20445-16-3

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20445-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20445-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,4 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20445-16:
(7*2)+(6*0)+(5*4)+(4*4)+(3*5)+(2*1)+(1*6)=73
73 % 10 = 3
So 20445-16-3 is a valid CAS Registry Number.

20445-16-3Downstream Products

20445-16-3Relevant academic research and scientific papers

NMR analysis of chiral alcohols and amines: Development of an environmentally benign "in tube" procedure with high efficiency and improved detection limit

Orlov, Nikolay V.,Ananikov, Valentine P.

supporting information; experimental part, p. 1735 - 1744 (2011/09/13)

A fast and efficient approach was developed for the NMR analysis of chiral alcohols and amines using readily available enantiopure MPA (α-methoxy- α-phenylacetic acid) and MTPA (α-methoxy-α- trifluoromethylphenylacetic acid) as chiral derivatizing agents. The procedure requires less than 5 min (including sample preparation time) for analysis using routine NMR hardware and allows accurate measurements for 0.01 mg of the sample of chiral compounds. Direct "in tube" analysis can be performed with high efficiency to determine enantiomeric purity and absolute configuration, as well as to monitor reactions in asymmetric synthesis and catalysis. The developed procedure is superior in terms of waste-free analysis of chiral compounds for environmentally benign applications.

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