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Ethyl-3-(2,4-dinitrophenylhydrazono)-4,4,4-trifluorobutanoate is a complex organic compound with the chemical formula C12H14F3N4O6. It is a derivative of ethyl 4,4,4-trifluorobutanoate, where the carboxylic acid group has been converted into a hydrazone with 2,4-dinitrophenylhydrazine. ethyl-3-(2,4-dinitrophenylhydrazono)-4,4,4-trifluorobutanoate is characterized by the presence of a trifluoromethyl group, which imparts unique chemical and physical properties due to the electron-withdrawing nature of fluorine atoms. The 2,4-dinitrophenylhydrazone moiety is a common functional group used in organic synthesis and analytical chemistry for the detection and quantification of aldehydes and ketones. The compound may be used in research settings for the study of reaction mechanisms, the synthesis of pharmaceuticals, or as a reagent in analytical procedures. Its specific applications and properties would depend on the context in which it is used, and it is important to handle such compounds with care due to their potential reactivity and the presence of nitro groups, which can be explosive under certain conditions.

1692-08-6

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1692-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1692-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1692-08:
(6*1)+(5*6)+(4*9)+(3*2)+(2*0)+(1*8)=86
86 % 10 = 6
So 1692-08-6 is a valid CAS Registry Number.

1692-08-6Downstream Products

1692-08-6Relevant academic research and scientific papers

Design, synthesis and biological evaluation of ethyl-4,4,4-trifluoro-3-hydrazonobutanoate derivatives

Abarbri, Mohamed,Alghamdi, Othman A.,Bougatef, Ali,Bougatef, Hajer,Jismy, Badr,Kossentini, Mohamed,Miled, Nabil,Saadaoui, Ikram,Salah, Bochra Ben

, (2021/10/29)

The present study describes the synthesis and biological investigation of novel ethyl 4,4,4-trifluoro-3-hydrazonobutanoate derivatives, which were synthesized by condensation of commercially available hydrazines and ethyl 4,4,4-trifluorobut-2-ynoate. We e

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