1107-69-3

Basic information

• Product Name: Propanal,2-[2-(2,4-dinitrophenyl)hydrazinylidene]-, 2-(2,4-dinitrophenyl)hydrazone
• Synonyms: Propanal,2-[(2,4-dinitrophenyl)hydrazono]-, (2,4-dinitrophenyl)hydrazone (9CI);Pyruvaldehyde, bis[(2,4-dinitrophenyl)hydrazone] (6CI,7CI,8CI);1,2-Propanedione bis(2,4-dinitrophenylhydrazone); Methylglyoxalbis[(2,4-dinitrophenyl)hydrazone]
• CAS NO: 1107-69-3
• Molecular Formula: C15H12 N8 O8
• Molecular Weight: 432.309
• Mol File: 1107-69-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Propanal,2-[2-(2,4-dinitrophenyl)hydrazinylidene]-, 2-(2,4-dinitrophenyl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Propanal,2-[2-(2,4-dinitrophenyl)hydrazinylidene]-, 2-(2,4-dinitrophenyl)hydrazone(1107-69-3)
• EPA Substance Registry System: Propanal,2-[2-(2,4-dinitrophenyl)hydrazinylidene]-, 2-(2,4-dinitrophenyl)hydrazone(1107-69-3)

Safety Data

• Hazardous Substances Data: 1107-69-3(Hazardous Substances Data)

Upstream product

• 91-22-5 quinoline 
• 71094-29-6 2.4-Dinitro-phenylhydrazon des Chloracetons 
• 54420-11-0 1,3-dihydroxy-acetone-(2,4-dinitro-phenylhydrazone) 
• 69864-54-6 α-acetyloxyacrolein 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 107-02-8 acrolein 
• 225793-59-9 2,4,6-triacetyl-1,3,5-trioxane 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 7803-57-8 hydrazine hydrate 
• 64-19-7 acetic acid 
• 7647-01-0 hydrogenchloride 
• 142-10-9 DL-glyceraldehyde 3-phosphate 
• 1567-89-1 N-(2,4-dinitrophenyl)-N'-isopropylidene-hydrazine 
• 32195-45-2 1,3-Dimesyloxy-2-(p-chlorphenylthio)-propan 

Relevant articles and documents

Hydrolysis of 2-alkoxyalk-2-enals

Hydrolysis of 2-alkoxyalk-2-enals with equimolar amount of water (in an organic solvent) and with an excess of water has been studied with the aim of synthesizing 2-oxopropanal (methylglyoxal). 2-Oxopropanal obtained in an excess of water exists in the hy

COMPARATIVE REACTIVITY OF α-ACETOXYACROLEIN AND α-ETHOXYACROLEIN

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KINETICS AND MECHANISM OF THE REDOX REACTION OF THALLIC SULPHATE WITH ACROLEINE

The stoichiometry, kinetics and mechanism of the redox reaction of thallic sulphate with acroleine in aqueous sulphuric acid or in aqueous dioxane solutions were studied.The acroleine molecule is oxidised with Tl(III) ions in two consecutive one-electron step to glyceraldehyde.The corresponding rate equation is -d/dt = kn , where n = 0-2.The zeroth reaction order with respect to thallic ions is attributed to a slow enolization of the hydrated acroleine, which is the rate-determining step preceding the redox reaction proper.