1166-15-0

Basic information

• Product Name: 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon
• Synonyms: 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon
• CAS NO: 1166-15-0
• Molecular Weight: 330.3
• Mol File: 1166-15-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon(1166-15-0)
• EPA Substance Registry System: 4-Aethoxy-benzaldehyd-2.4-dinitro-phenylhydrazon(1166-15-0)

Safety Data

• Hazardous Substances Data: 1166-15-0(Hazardous Substances Data)

Upstream product

• 10031-82-0 4-ethoxybenzaldehyde 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 

Downstream Products

• 10031-82-0 4-ethoxybenzaldehyde 

Relevant articles and documents

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

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.