255896-36-7

Basic information

• Product Name: Methanone, (4,5-dimethoxy-2-nitrophenyl)phenyl-
• CAS NO: 255896-36-7
• Molecular Formula: C15H13NO5
• Molecular Weight: 287.272
• Mol File: 255896-36-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanone, (4,5-dimethoxy-2-nitrophenyl)phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4,5-dimethoxy-2-nitrophenyl)phenyl-(255896-36-7)
• EPA Substance Registry System: Methanone, (4,5-dimethoxy-2-nitrophenyl)phenyl-(255896-36-7)

Safety Data

• Hazardous Substances Data: 255896-36-7(Hazardous Substances Data)

Upstream product

• 179104-60-0 α-phenyl-4,5-dimethoxy-2-nitrobenzyl alcohol 
• 98-88-4 benzoyl chloride 
• 91-16-7 1,2-dimethoxybenzene 
• 4038-14-6 3,4-dimethoxybenzophenone 

Downstream Products

• 101584-85-4 acetic acid-(2-benzyl-4,5-dimethoxy-anilide) 
• 2041-27-2 2,3-Dimethoxyfluoren-9-one 
• 309927-66-0 4-[5,6-dimethoxy-1-(4-methylphenylsulfonyl)-3-phenyl-1H-2-indolyl]-2-butanone 
• 340696-26-6 2-[5-ethyl-2-furyl(phenyl)methyl]-4,5-dimethoxy-1-(4-methylphenylsulfonamido)benzene 
• 309927-65-9 4-methyl-N-{4,5-dimethoxy-2-[(5-methylfuran-2-yl)(phenyl)methyl]phenyl}benzenesulfonamide 
• 340696-16-4 N-(4,5-dimethoxy-2-(hydroxy(phenyl)methyl)phenyl)-4-methylbenzenesulfonamide 
• 873984-49-7 2-benzoyl-4,5-dimethoxy-1-phenylcarboxamidobenzene 
• 924635-61-0 4,5-dimethoxy-2-[5-(4-methylphenyl)-2-furyl(phenyl)methyl]-1-(4-methylphenylsulfonamido)benzene 
• 924635-59-6 2-[5-(tert-butyl)-2-furyl(phenyl)methyl]-4,5-dimethoxy-1-(4-methylphenylsulfonamido)benzene 
• 924635-67-6 4,5-dimethoxy-2-[5-methyl-2-furyl(phenyl)methyl]-1-phenylcarboxamidobenzene 
• 924635-68-7 N-{2-[5-(tert-butyl)-2-furyl(phenyl)methyl]-4,5-dimethoxyphenyl}acetamide 
• 309927-64-8 2-benzoyl-4,5-dimethoxy-1-(4-methylphenylsulfonamido)benzene 
• 924635-66-5 N-{4,5-dimethoxy-2-[5-methyl-2-furyl(phenyl)methyl]phenyl}methanesulfonamide 
• 924635-65-4 2-hydroxy(phenyl)methyl-4,5-dimethoxy-1-phenylcarboxamidobenzene 

Relevant articles and documents

Artificial Molecular Pump Operating in Response to Electricity and Light

The ability to control the relative motions of component parts in molecules is essential for the development of molecular nanotechnology. The advent of mechanically interlocked molecules (MIMs) has enhanced significantly the opportunities for chemists to harness such motions in artificial molecular machines (AMMs). Recently, we have developed artificial molecular pumps (AMPs) capable of producing highly energetic oligo- and polyrotaxanes with high precision. Here, we report the design, synthesis, and operation of an AMP incorporating a photocleavable stopper that allows for the use of orthogonal stimuli. Our approach employs a ratchet mechanism to pump a ring onto a collecting chain, forming an intermediate [2]rotaxane. At a subsequent time, application of light triggers the release of the ring back into the bulk solution with temporal control. This process is monitored by the quenching of the fluorescence of a naphthalene-based fluorophore. This design may find application in the fabrication of molecular transporting systems with on-demand functions.

Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction

A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.