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4-Ethoxy-benzaldehyde-2,4-dinitro-phenylhydrazon is a complex organic compound that serves as a derivative of benzaldehyde. It is characterized by the presence of an ethoxy group (C2H5O-) attached to the 4-position of the benzene ring, and a 2,4-dinitro-phenylhydrazone moiety. The latter is formed by the reaction of benzaldehyde with 2,4-dinitrophenylhydrazine, resulting in a Schiff base. 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon is of interest in chemical research and may have potential applications in the synthesis of various organic compounds due to its unique structure and reactivity. It is important to note that the handling and use of such chemicals should be done with caution, adhering to proper safety protocols, as they can be sensitive to various reaction conditions and may have specific hazard profiles.

1166-15-0

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1166-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1166-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1166-15:
(6*1)+(5*1)+(4*6)+(3*6)+(2*1)+(1*5)=60
60 % 10 = 0
So 1166-15-0 is a valid CAS Registry Number.

1166-15-0Downstream Products

1166-15-0Relevant academic research and scientific papers

Studies on the kinetics of tripropylammonium fluorochromate oxidation of some aromatic alcohols in non-aqueous media

Mansoor, S. Sheik,Shafi, S. Syed

, p. 85 - 90 (2010)

The oxidation of benzyl alcohol (BnOH) and a few para-substituted benzyl alcohols by tripropylammonium fluorochromate (TriPAFC) in dimethylsulphoxide (DMSO) leads to the formation of corresponding aldehydes. The reaction is first order each in TriPAFC and the alcohols. The reaction is catalysed by hydrogen ions. The hydrogen ion dependence has the form: kobs = a + b[H +]. The oxidation of α α′-dideuterio benzyl alcohol exhibited a substantial primary kinetic isotope effect (kH/k D = 5.45 at 303 K). Oxidation of benzyl alcohol was studied in 19 different organic solvents. The solvent effect has been analysed using Kamlet's and Swain's multiparametric equation. A mechanism involving a hydride ion transfer via chromate ester is proposed.

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