62507-47-5

Basic information

• Product Name: Methanone, (3-methoxyphenyl)(4-nitrophenyl)-
• Synonyms: 3-methoxy-4'-nitrobenzophenone;3-methoxyl-4'-nitrobenzophenone
• CAS NO: 62507-47-5
• Molecular Formula: C14H11NO4
• Molecular Weight: 257.246
• Mol File: 62507-47-5.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Methanone, (3-methoxyphenyl)(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (3-methoxyphenyl)(4-nitrophenyl)-(62507-47-5)
• EPA Substance Registry System: Methanone, (3-methoxyphenyl)(4-nitrophenyl)-(62507-47-5)

Safety Data

• Hazardous Substances Data: 62507-47-5(Hazardous Substances Data)

Upstream product

• 1711-05-3 m-anisoyl chloride 
• 79048-32-1 4-(tri-n-butylstannyl)nitrobenzene 
• 18927-05-4 methyl (3-methoxyphenyl)acetate 
• 98-95-3 nitrobenzene 
• 636-98-6 p-nitrobenzene iodide 
• 201230-82-2 carbon monoxide 
• 10365-98-7 3-methoxyphenylboronic acid 
• 591-31-1 3-methoxy-benzaldehyde 
• 350-46-9 4-Fluoronitrobenzene 
• 122-04-3 4-nitro-benzoyl chloride 
• 100-66-3 methoxybenzene 
• 122439-11-6 tributyl(3-methoxyphenyl)stannane 
• 123567-57-7 α-(3-methoxyphenyl)-4-morpholineacetonitrile 

Downstream Products

• 147029-63-8 Acetic acid (2S,3R,4S,5R)-4,5-diacetoxy-2-[3-(4-nitro-benzoyl)-phenoxy]-tetrahydro-pyran-3-yl ester 
• 83355-06-0 (4-Nitro-phenyl)-[3-((2S,3R,4S,5R)-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-phenyl]-methanone 
• 147029-77-4 4'-nitro-3-hydroxybenzophenone 

Relevant articles and documents

Recyclable polyetheretherketone fiber-supported N-heterocyclic carbene catalysts for nucleophilic acylation of fluorobenzenes

We report for the first time a novel support of polyetheretherketone fiber for the synthesis of recyclable N-heterocyclic carbene (NHC) catalysts. The fiber catalysts were verified in nucleophilic acylation of fluorobenzenes with superior catalytic activities, and successfully recycled by a tiny pair of tweezers over 21 cycles with minimal loss of performance.

Total Synthesis of Termicalcicolanone A via Organocatalysis and Regioselective Claisen Rearrangement

A total synthesis of an anticancer xanthone natural product termicalcicolanone A utilizing multiple nucleophilic aromatic substitutions and pericyclic reactions has been developed. The pyrano[3,2-b]xanthen-6-one scaffold was constructed via NHC-catalyzed

Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: Facile access to diarylketones

A facile and regioselective base-mediated aerobic oxidative acylation of nitroarenes to access diarylketones under mild conditions has been developed. It features the use of bench-stable and readily available arylacetates as acyl surrogates, and the absence of transition-metals and synthetic oxidants. This protocol involves a cascade CDC/oxidative decarboxylation process.