52507-17-2

Basic information

• Product Name: 5(4H)-Oxazolone, 4-[[4-(acetyloxy)phenyl]methylene]-2-methyl-
• CAS NO: 52507-17-2
• Molecular Formula: C13H11NO4
• Molecular Weight: 245.235
• Mol File: 52507-17-2.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: 5(4H)-Oxazolone, 4-[[4-(acetyloxy)phenyl]methylene]-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 5(4H)-Oxazolone, 4-[[4-(acetyloxy)phenyl]methylene]-2-methyl-(52507-17-2)
• EPA Substance Registry System: 5(4H)-Oxazolone, 4-[[4-(acetyloxy)phenyl]methylene]-2-methyl-(52507-17-2)

Safety Data

• Hazardous Substances Data: 52507-17-2(Hazardous Substances Data)

Upstream product

• 127-09-3 sodium acetate 
• 108-24-7 acetic anhydride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 543-24-8 N-acetylglycine 
• 878-00-2 4-formylphenyl acetate 
• 71428-89-2 N-crotonylglycine 
• 124-40-3 dimethyl amine 
• 24474-93-9 2-methyl-4H-oxazol-5-one 
• 69932-90-7 N-benzylsulfanylcarbonyl-glycine 
• 56-40-6 glycine 
• 1145-56-8 2-(2-chloroacetamido)-3-(4-hydroxyphenyl)propanoic acid 

Downstream Products

• 52507-28-5 α-Acetylamino-p-hydroxy-zimtsaeuremethylester 
• 70529-59-8 N,O-diacetyltyrosine azlactone 
• 80630-63-3 N-(N,O-diacetyldehydrotyrosyl)-(R)-alanine methyl ester 
• 200940-00-7 (Z)-4-(4-hydroxybenzylidene)-1,2-dimethyl-1H-imidazol-5(4H)-one 
• 52507-19-4 p-(2-Acetylaminovinyl)-acetoxybenzol 
• 58848-83-2 3,4-dihydro-6-(4-hydroxybenzyl)-3-sulfanyl-1,2,4-triazin-5(2H)-one 
• 60470-84-0 methyl (Z)-2-acetamido-3-(4-acetoxyphenyl)acrylate 
• 1450880-87-1 (Z)-tert-butyldiphenylsilyl 4-(4-(4-((tert-butyldiphenylsilyl)-oxy)benzylidene)-2-methyl-5-oxo-4,5-dihydro-1H-imidazol-1-yl)butanoate 
• 73043-35-3 (Z)-4-(4-(4-hydroxybenzylidene)-2-methyl-5-oxo-4,5-dihydro-1H-imidazole-1-yl)butanoic acid 
• 1446876-37-4 C₁₉H₂₄N₂O₄ 
• 1446876-44-3 C₁₇H₂₀N₂O₃ 
• 1446876-39-6 C₁₉H₂₃BrN₂O₄ 
• 1384247-32-8 4-(4-hydroxybenzylidene)-1-benzyl-2-methylimidazol-5-one 

Relevant articles and documents

Evidence of the structure of 4-(4′-acetoxybenzylidene)-2-methyl-5-oxazolone and its phenylpropenoic acid derivatives

4-(4′-Acetoxybenzylidine)-2-methyl-5-oxazolone (Z-isomer) was synthesized, which upon basic hydrolysis yielded the unexpected 2-acetoxy-3-(p-hydroxyphenyl)-propenoic acid and treatment with acetic acid formed 2-acetoxy-3-(p-acetoxyphenyl)-propenoic acid. The structures of the three compounds were assigned by NMR spectroscopy. An X-ray crystallographic study of the starting azlactone confirmed its structure and supported the fact that the Z-configuration was retained during the synthesis of the phenylpropenoic acid derivatives.

An Atropos Chiral Biphenyl Bisphosphine Ligand Bearing Only 2,2′-Substituents and Its Application in Rh-Catalyzed Asymmetric Hydrogenation

An atropos chiral biphenyl bisphosphine ligand bearing only 2,2′-substituents was rationally designed and easily synthesized utilizing a bulky chiral t-butylmethylphosphino block. Computational results showed a large difference in the free energies betwee

New compounds having skin whitening, antioxidant and PPAR activity, and medical use thereof

PURPOSE: A novel compound with skin whitening, antioxidation, and PPAR activation effects, and a medical use thereof are provided to be used for a pharmaceutical composition or a cosmetic product. CONSTITUTION: A compound is denoted by chemical formula 1. A skin whitening composition contains the compound as an active ingredient. An antioxidative composition for preventing or treating oxidative diseases contains the compound of chemical formula 1 as an active ingredient. The oxidative diseases are selected among skin aging, pigmentation, wrinkling, psoriasis, or eczema. The composition prevents or treats diseases which are regulated by PPAR(peroxisome proliferator-activated receptor) activity. The PPAR includes PPAR alpha or PPAR gamma.