3618-76-6

Basic information

• Product Name: Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester
• CAS NO: 3618-76-6
• Molecular Formula: C10H10N4O6
• Molecular Weight: 282.213
• Mol File: 3618-76-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester(3618-76-6)
• EPA Substance Registry System: Propanoic acid, 2-[(2,4-dinitrophenyl)hydrazono]-, methyl ester(3618-76-6)

Safety Data

• Hazardous Substances Data: 3618-76-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 790-12-5 2-(2,4-dinitrophenylhydrazono)-propanoic acid 
• 600-22-6 pyruvic acid methyl ester 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 186581-53-3 diazomethane 
• 123-54-6 acetylacetone 
• 75-91-2 tert.-butylhydroperoxide 
• 3153-26-2 bis(acetylacetonate)oxovanadium 
• 368-84-3 4-methyl-2-trifluoromethyl-1,3-oxazol-5-one 

Downstream Products

• 78178-96-8 methyl bromopyruvate 2,4-dinitrophenylhydrazone 
• 83289-24-1 methyl (1α,12bα,Z)-α-<(2,4-dinitrophenyl)hydrazono>-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizine-1-propanoate 
• 83289-23-0 methyl (1β,12bβ,Z)-α-<(2,4-dinitrophenyl)hydrazono>-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizine-1-propanoate 
• 83289-22-9 methyl (+/-)-(1α,12bα,Z)-α-<(2,4-dinitrophenyl)hydrazono>-1-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizine-1-propanoate 
• 78179-02-9 1-<2-<(2,4-dinitrophenyl)hydrazono>-2-(methoxycarbonyl)ethyl>-1-ethyl-2,3,4,6,7,12-hexahydro-1H-indolo<2,3-a>quinolizin-5-ium bromide 

Relevant articles and documents

Reactions of hydroxyl-containing compounds with tert-butyl hydroperoxide in the presence of chromium tetra-tert-butoxide

Primary and secondary aliphatic, alkylaromatic, cyclic, and organoelement alcohols are efficiently oxidized by tert-butyl hydroperoxide in the presence of both equimolar and catalytic quantities of chromium tetra-tert-butoxide (C6H6, 20°C). α-Diols containing tertiary hydroxyl groups interact with this system via oxidative splitting of the carbon scaffold. The oxidation includes the stages of formation and decomposition of chromium-containing peroxy compounds. Further transformations of the carbonyl compounds depend on the structure of radicals in the molecules.

Synthesis of vincamine

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