53073-02-2

Basic information

• Product Name: sodium salt of p-toluoylacetaldehyde
• Synonyms: sodium salt of p-toluoylacetaldehyde
• CAS NO: 53073-02-2
• Molecular Weight: 184.17
• Mol File: 53073-02-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: sodium salt of p-toluoylacetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: sodium salt of p-toluoylacetaldehyde(53073-02-2)
• EPA Substance Registry System: sodium salt of p-toluoylacetaldehyde(53073-02-2)

Safety Data

• Hazardous Substances Data: 53073-02-2(Hazardous Substances Data)

Upstream product

• 122-00-9 para-methylacetophenone 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 18103-98-5 3-dimethylamino-1-(4-methyl-phenyl)-2-propen-1-one 
• 17263-64-8 2-diazo-1-(4-methylphenyl)ethanone 
• 24477-67-6 Bis<2-(p-toluoyl)vinyl>-aether 
• 53009-33-9 5-p-Tolyl-4,5-dihydro-isoxazol-5-ol 
• 54556-93-3 Phosphoric acid (Z)-3-oxo-3-p-tolyl-propenyl ester diphenyl ester 
• 130340-22-6 Benzoic acid [(Z)-3-hydroxy-3-p-tolyl-prop-2-en-(E)-ylidene]-hydrazide 
• 130340-25-9 4-Chloro-benzoic acid [(Z)-3-hydroxy-3-p-tolyl-prop-2-en-(E)-ylidene]-hydrazide 
• 137621-85-3 2-(1,3-dithiolane-2-ylidene)-3-(4-methylphenyl)-3-oxopropanal 
• 138722-03-9 5-Benzoyl-3-(4-methylbenzoyl)-2-(phenacylthio)thiophene 
• 130340-23-7 4-Methyl-benzoic acid [(Z)-3-hydroxy-3-p-tolyl-prop-2-en-(E)-ylidene]-hydrazide 
• 138696-49-8 2-(4-methylbenzoyl)-3,3-bis(methylsulfanyl)acrylaldehyde 
• 41877-77-4 (2Z,4Z)-2-Cyano-5-hydroxy-5-p-tolyl-penta-2,4-dienoic acid ethyl ester 
• 62090-41-9 C₁₃H₁₂N₂O₂ 
• 130340-37-3 (5-Hydroxy-5-p-tolyl-4,5-dihydro-pyrazol-1-yl)-phenyl-methanone 

Relevant articles and documents

Effect of Diamine Bridge on Reactivity of Tetradentate ONNO Nickel(II) Complexes

Two new square planar ONNO nickel(II) complexes C2_core and C3_core have been synthesized and characterized by single crystal X-ray diffraction, NMR spectroscopy, thermogravimetry, and DFT calculations. The experimental results revealed the effect of the length of diamine bridge in the ligand on the behavior of the studied complexes in the reaction with N-heterocyclic aromatic amines, while DFT calculations provided a basis for the rationalization of this observation. The complex with propylenediamine bridge (C3_core) readily reacts with pyridine and its derivatives to form high-spin (paramagnetic) complexes with octahedral geometry as characterized by X-ray diffraction; electron-donating substituents on the pyridine ring facilitate the coordination of axial ligands. In contrast, the complex with ethylenediamine bridge (C2_core) does not undergo such a reaction because of the high deformation energy of the core required for the formation of C2_Py complex.