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methyl 3-hydroxy-4,4,4-trifluorobutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

475467-53-9

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475467-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475467-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,4,6 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 475467-53:
(8*4)+(7*7)+(6*5)+(5*4)+(4*6)+(3*7)+(2*5)+(1*3)=189
189 % 10 = 9
So 475467-53-9 is a valid CAS Registry Number.

475467-53-9Downstream Products

475467-53-9Relevant academic research and scientific papers

Synthesis method of 2-pyrazine carboxylic ester compound

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Paragraph 0038-0041; 0106-0109; 0113, (2021/04/14)

The invention provides a synthetic method of a 2-pyrazine carboxylic ester compound. The synthesis method comprises the following steps: S1, carrying out addition reaction on a compound 1 and glyoxal dioxime under the action of a Lewis acid catalyst to obtain an intermediate 1; and step S2, carrying out first dehydration reaction on the intermediate 1 to obtain the 2-pyrazine carboxylic ester compound, wherein the structural general formulas of the compound 1, the intermediate 1 and the 2-pyrazine carboxylic ester compound are sequentially shown in the specification, R1 being a C1-C15 substituted or unsubstituted alkyl group, and R2 being a C1-C10 alkyl group. The preparation cost (or commercially available price) of the initial raw material compound 1 adopted by the invention is generally far lower than that of a trifluoropyruvate methyl ester compound. Compared with the traditional preparation method of 3-trifluoromethyl-2-methyl pyrazinecarboxylate, the method has the advantages of mild reaction conditions, simple operation and wide raw material sources, avoids the use of an expensive coupling catalyst, and greatly reduces the cost.

Process for producing optically active alcohol

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, (2008/06/13)

A novel production process capable of obtaining an optically active alcohol in a high optical purity by subjecting a β-keto ester such as a 3-perfluoroalkyl-3-oxopropionate ester or a 3-trichloroalkyl-3-oxopropionate ester to asymmetric reduction in simple and convenient operations.

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