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L-Phenylalanine, N-(trifluoroacetyl)-, ethyl ester is a chemical compound with the molecular formula C12H12F3NO3. It is a derivative of the amino acid L-phenylalanine, where the nitrogen atom is acylated with a trifluoroacetyl group, and the carboxylic acid group is esterified with an ethyl group. L-Phenylalanine, N-(trifluoroacetyl)-, ethyl ester is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoroacetyl group, provides it with specific reactivity and properties that can be exploited in chemical transformations. The ethyl ester functionality allows for controlled hydrolysis under certain conditions, making it a versatile building block in the synthesis of more complex molecules.

2563-33-9

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2563-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2563-33-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2563-33:
(6*2)+(5*5)+(4*6)+(3*3)+(2*3)+(1*3)=79
79 % 10 = 9
So 2563-33-9 is a valid CAS Registry Number.

2563-33-9Relevant academic research and scientific papers

The enzyme-catalysed stereoselective transesterification of phenylalanine derivatives in supercritical carbon dioxide

Smallridge, Andrew J.,Trewhella, Maurie A.,Wang

, p. 259 - 262 (2007/10/03)

The subtilisin Carlsberg catalysed transesterification of N-acetyl phenylalanine methyl ester (1), N-acetyl phenylalanine ethyl ester (2), N-trifluoroacetyl phenylalanine methyl ester (3) and N-trifluoroacetyl phenylalanine ethyl ester (4) was studied in supercritical carbon dioxide. The water content of the reaction affects the reactivity of the system; for the transesterification of the methyl esters with ethanol the optimum concentration of water was determined to be about 0.74 M, while for the transesterification of the ethyl esters with methanol the optimum concentration of water was about 1.3 M. The conversion is also dependent upon the concentration of alcohol; for ethanol, 2% v/v gives the maximum conversion, whilst for methanol, only 0.8-1. 2% v/v is required. This is probably due to a difference in the solubility of the substrates in the two alcohol/supercritical carbon dioxide mixtures. The reaction is highly stereoselective, in all cases no evidence for reaction of the D-isomer could be detected by chiral gas chromatography.

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