711015-30-4

Basic information

• Product Name: 2-methyl-4-[(E)-(4-nitrophenyl)methylidene]-1,3-oxazol-5(4H)-one
• Synonyms: 2-methyl-4-[(E)-(4-nitrophenyl)methylidene]-1,3-oxazol-5(4H)-one
• CAS NO: 711015-30-4
• Molecular Weight: 232.196
• Mol File: 711015-30-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-methyl-4-[(E)-(4-nitrophenyl)methylidene]-1,3-oxazol-5(4H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-4-[(E)-(4-nitrophenyl)methylidene]-1,3-oxazol-5(4H)-one(711015-30-4)
• EPA Substance Registry System: 2-methyl-4-[(E)-(4-nitrophenyl)methylidene]-1,3-oxazol-5(4H)-one(711015-30-4)

Safety Data

• Hazardous Substances Data: 711015-30-4(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 66949-13-1 (Z)-2-methyl-4-(4-nitrobenzylidene)oxazol-5(4H)-one 
• 543-24-8 N-acetylglycine 

Downstream Products

• 117499-10-2 N-(carboxymethyl)-N-(2-(bis(carboxymethyl)amino)ethyl)-3-(4-aminophenyl)alanine 
• 117499-12-4 N-(carboxymethyl)-N-(2-(bis(carboxymethyl)amino)ethyl)-3-(4-isothiocyanatophenyl)alanine dihydrochloride 
• 117499-14-6 N-(2-aminoethyl)-3-(4-nitrophenyl)alanine dihydrochloride 
• 117499-15-7 N-(carboxymethyl)-N-(2-(bis(carboxymethyl)amino)ethyl)-3-(4-nitrophenyl)alanine 
• 38335-24-9 3-(4-nitrophenyl)-2-oxopropanoic acid 
• 123944-82-1 methyl 2-hydroxy-3-(4-nitrophenyl)propionate 
• 141666-15-1 2-hydroxy-3-(4-nitrophenyl)-2-propenoic acid 
• 1081844-77-0 (2E)-2-(acetylamino)-3-(4-nitrophenyl)prop-2-enoic acid 
• 140935-44-0 2-(Benzothiazol-2-ylsulfanyl)-N-{2-methyl-4-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-5-oxo-4,5-dihydro-imidazol-1-yl}-acetamide 
• 140935-54-2 2-(Benzooxazol-2-ylsulfanyl)-N-{2-methyl-4-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-5-oxo-4,5-dihydro-imidazol-1-yl}-acetamide 

Relevant articles and documents

Benzylidene-oxazolones as photoswitches: Photochemistry and theoretical calculations

The photophysics and photochemistry of a family of compounds proposed as efficient molecular photoswitches is presented. The effect of different light sources, substituents and solvents in the photostationary state has been explored. A detailed mechanisti

Oxazolones: New tyrosinase inhibitors; synthesis and their structure-activity relationships

The tyrosinase inhibitory potential of seventeen synthesized oxazolone derivatives has been evaluated and their structure-activity relationships developed in the present work. All the synthesized derivatives, 3-19, demonstrated excellent in vitro tyrosina

Chemocontrolled reduction of aromatic α-ketoesters by NaBH4: Selective synthesis of α-hydroxy esters or 1,2-diols

α-Hydroxyesters 5a-g or diols 6a-g have been obtained in high yields by reduction of aromatic α-ketoesters 4 once or twice respectively by using NaBH4 as the reducer under suitable conditions. The use of a solvent that does not interact with the reagent allowed the double reduction to occur with only a slight excess of borohydride in very mild conditions.