51042-54-7

Basic information

• Product Name: Benzene, 1,2-dimethoxy-4-[(1E)-2-(4-nitrophenyl)ethenyl]-
• CAS NO: 51042-54-7
• Molecular Formula: C16H15NO4
• Molecular Weight: 285.299
• Mol File: 51042-54-7.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2-dimethoxy-4-[(1E)-2-(4-nitrophenyl)ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2-dimethoxy-4-[(1E)-2-(4-nitrophenyl)ethenyl]-(51042-54-7)
• EPA Substance Registry System: Benzene, 1,2-dimethoxy-4-[(1E)-2-(4-nitrophenyl)ethenyl]-(51042-54-7)

Safety Data

• Hazardous Substances Data: 51042-54-7(Hazardous Substances Data)

Upstream product

• 104-03-0 4-nitrobenzeneacetic acid 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 51042-50-3 4-nitrobenzyltriphenylarsonium bromide 
• 121682-44-8 N-<1-(4-nitrophenyl)-2-(3,4-dimethoxyphenyl)ethyl>formamide 
• 121682-41-5 N-<1-(3,4-dimethoxyphenyl)-2-(4-nitrophenyl)ethyl>formamide 
• 121682-42-6 N-<1-(3,4-dimethoxyphenyl)-2-(4-nitrophenyl)ethyl>acetamide 
• 110-89-4 piperidine 
• 100-13-0 4-nitrostyrene 
• 5460-32-2 1-iodo-3,4-dimethoxybenzene 
• 619-73-8 4-nitrobenzyl chloride 
• 555-16-8 4-nitrobenzaldehdye 
• 2609-49-6 diethyl p-nitrobenzylphosphonate 
• 6380-23-0 3,4-dimethoxystyrene 
• 100-00-5 4-chlorobenzonitrile 

Downstream Products

• 110997-83-6 4-[2-(3,4-dimethoxyphenyl)ethyl]aniline 
• 874988-46-2 1,2-dimethoxy-4-((4-nitrophenyl)ethynyl)benzene 
• 874988-44-0 4-[1,2-Dibromo-2-(4-nitro-phenyl)-ethyl]-1,2-dimethoxy-benzene 

Relevant articles and documents

Nonlinear optical properties of diaromatic stilbene, butadiene and thiophene derivatives

Series of highly polar stilbene (1a-e), diphenylbutadiene (2a-c) and phenylethenylthiophene (3a-c) derivatives were preparedviaHorner-Wadsworth-Emmons method with a view to produce new and efficient materials for second harmonic generation (SHG) in the so

Discovery of efficient stimulators for adult hippocampal neurogenesis based on scaffolds in dragon's blood

Reduction of hippocampal neurogenesis caused by aging and neurological disorders would impair neural circuits and result in memory loss. A new lead compound (N-trans-3′,4'-methylenedioxystilben-4-yl acetamide 27) has been discovered to efficiently stimulate adult rats' neurogenesis. In-depth structure-activity relationship studies proved the necessity of a stilbene scaffold that is absent in highly cytotoxic analogs such as chalcones and heteroaryl rings and inactive analogs such as diphenyl acetylene and diphenyl ethane, and validated the importance of an NH in the carboxamide and a methylenedioxy substituent on the benzene ring. Immunohistochemical staining and biochemical analysis indicate, in contrast to previously reported neuroprotective chemicals, N-stilbenyl carboxamides have extra capacity for neuroproliferation-type neurogenesis, thereby providing a foundation for improving the plasticity of the adult mammalian brain.

Mechanically activated synthesis of (E)-stilbene derivatives by high-speed ball milling

An efficient mechanically activated solvent-free synthesis of (E)-stilbene derivatives by high-speed ball milling is described. This method has notable advantages in terms of good yield, short reaction time and high selectivity. Copyright