198063-87-5

Basic information

• Product Name: Methyl 3-[2-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrrol-3-yl]propanoate
• Synonyms: Methyl 3-[2-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrrol-3-yl]propanoate
• CAS NO: 198063-87-5
• Molecular Formula: C₁₃H₁₁Cl₂NO₃
• Molecular Weight: 279.71886
• Mol File: 198063-87-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 3-[2-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrrol-3-yl]propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 3-[2-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrrol-3-yl]propanoate(198063-87-5)
• EPA Substance Registry System: Methyl 3-[2-(4-chlorophenyl)-5-oxo-4,5-dihydro-1H-pyrrol-3-yl]propanoate(198063-87-5)

Safety Data

• Hazardous Substances Data: 198063-87-5(Hazardous Substances Data)

Upstream product

• 198064-80-1 methyl 5-(4-chlorophenyl)-5-oxo-4-(phenyoxycarbonyloxy)pentanoate 
• 89150-43-6 methyl 4-bromo-5-(4-chlorophenyl)-5-oxopentanoate 
• 198064-79-8 methyl 5-(4-chlorophenyl)-4-hydroxy-5-oxopentanoate 
• 108-90-7 chlorobenzene 
• 71354-29-5 methyl 5-(4-chlorophenyl)-5-oxopentanoate 
• 1501-26-4 methyl 4-(chlorocarbonyl)butyrate 
• 198064-81-2 methyl 3-[4-(4-chlorophenyl)-2-oxo-2,3-dihydro-5-oxazolyl]propionate 

Downstream Products

• 1222011-01-9 methyl 3-[4-(4-chlorophenyl)-2-(1-propylsulfanyl)-5-oxazolyl]propionate 
• 198064-19-6 4-(4-chlorophenyl)-2-(4,5-dimethyl-1-imidazolyl)-5-oxazolepropionic acid 
• 198064-17-4 4-(4-chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-oxazolepropionic acid 
• 198064-20-9 3-[2-(1H-benzoimidazol-1-yl)-4-(4-chlorophenyl)-5-oxazolyl]propionic acid 
• 327188-45-4 methyl 4-(4-chlorophenyl)-2-(2-pyrimidinylsulfanyl)-5-oxazolepropionate 

Relevant articles and documents

Synthesis and biological activity of novel 5-(omega-aryloxyalkyl)oxazole derivatives as brain-derived neurotrophic factor inducers.

A novel series of 5-(omega-aryloxyalkyl)oxazole derivatives was prepared and their effects on brain-derived neurotrophic factor (BDNF) production were evaluated in human neuroblastoma (SK-N-SH) cells. Syntheses were performed by construction of an oxazole

Oxazole derivatives, their production and use

A novel compound of the formula: wherein R1 is a halogen atom, an optionally substituted heterocyclic, hydroxy, thiol or amino group; A is an optionally substituted acyl group, an optionally substituted heterocyclic group, an optionally substituted hydroxy group, or an optionally esterified or amidated carboxy group; B is an optionally substituted aromatic group; Y is a divalent aliphatic hydrocarbon group, or a salt thereof, which have an excellent insulin secertion-promoting and blood sugar-depressing effect, and useful in agents for diabetes.