91890-10-7

Basic information

• Product Name: Morpholine, 4-[1-(4-methoxyphenyl)ethenyl]-
• CAS NO: 91890-10-7
• Molecular Formula: C13H17NO2
• Molecular Weight: 219.283
• Mol File: 91890-10-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Morpholine, 4-[1-(4-methoxyphenyl)ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Morpholine, 4-[1-(4-methoxyphenyl)ethenyl]-(91890-10-7)
• EPA Substance Registry System: Morpholine, 4-[1-(4-methoxyphenyl)ethenyl]-(91890-10-7)

Safety Data

• Hazardous Substances Data: 91890-10-7(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 768-60-5 4-methoxyphenylacetylen 

Downstream Products

• 15118-67-9 ethyl 3-(4-methoxybenzoyl)-propionate 
• 73744-44-2 2-fluoro-4'-methoxyacetophenone 
• 114829-07-1 ω,ω-Difluoro-4-methoxyacetophenone 
• 64274-22-2 4-[4-methoxy-N-(toluene-4-sulfonyl)-benzimidoyl]-morpholine 
• 1443120-89-5 ethyl 6-(4-methoxyphenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate 
• 1443120-98-6 diethyl 2-(4-(4-methoxyphenyl)-4-oxobutan-2-ylidene)malonate 
• 1443120-90-8 ethyl 6-(4-methoxyphenyl)-2-oxo-4-propyl-1,2-dihydropyridine-3-carboxylate 
• 101790-35-6 methyl 4-oxo-4-(4-methoxy-phenyl)-2-phenyl-butanoate 
• 96921-36-7 N-[1-(4-methoxyphenyl)ethyl]morpholine 
• 1284281-59-9 4-bromo-1-(3-bromophenyl)-N-(4-cyanotetrahydro-2H-pyran-4-yl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxamide 
• 1284281-38-4 ethyl 4-bromo-1-(3-bromophenyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxylate 
• 1314017-94-1 C₁₇H₁₂Br₂N₂O₃ 
• 1284281-37-3 ethyl 1-(3-bromophenyl)-5-(4-methoxyphenyl)-1H-pyrazole-3-carboxylate 

Relevant articles and documents

Achieving Aliphatic Amine Addition to Arylalkynes via the Lewis Acid Assisted Triazole-Gold (TA-Au) Catalyst System

Transition metal catalyzed intermolecular hydroamination of the arylalkynes with aliphatic amine is generally problematic due to the good coordination between amine and metal cation. With the combination of 1,2,3-triazole coordinated gold(I) catalyst (TA-Au) and Zn(OTf)2 cocatalyst, this challenging transformation was achieved with good to excellent yields and regioselectivity. Compared to previously reported methods, this approach offered an alternative catalyst system to achieve this fundamental chemical transformation with high efficiency and practical conditions.

N -(4-cyanotetrahydro-2 H -pyran-4-yl) and N -(1-cyanocyclohexyl) derivatives of 1,5-diarylpyrazole-3-carboxamides showing high affinity for 18 kDa translocator protein and/or cannabinoid receptors

In order to develop improved radioligands for imaging brain CB1 receptors with positron emission tomography (PET) based on rimonabant (5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(piperidin-1-yl) -1H-pyrazole-3-carboxamide, 1), we synt

Reactions of enamines with selectfluor: A straightforward route to difluorinated carbonyl compounds

Reactions of enamines, preformed from β-dicarbonyl and monocarbonyl compounds, with Selectfluor (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2] octane bis(tetrafluoroborate) under mild conditions (triethylamine (TEA) or molecular sieves) easily led to the corresponding difluorinated carbonyl compounds in high yields.