38693-94-6

Basic information

• Product Name: Phenol, 4-[(1E)-2-(4-fluorophenyl)ethenyl]-
• CAS NO: 38693-94-6
• Molecular Formula: C14H11FO
• Molecular Weight: 214.239
• Mol File: 38693-94-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Phenol, 4-[(1E)-2-(4-fluorophenyl)ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[(1E)-2-(4-fluorophenyl)ethenyl]-(38693-94-6)
• EPA Substance Registry System: Phenol, 4-[(1E)-2-(4-fluorophenyl)ethenyl]-(38693-94-6)

Safety Data

• Hazardous Substances Data: 38693-94-6(Hazardous Substances Data)

Upstream product

• 405-99-2 para-fluorostyrene 
• 120506-39-0 (4-(bromomethyl)phenoxy) (tert-butyl) dimethylsilane 
• 138585-08-7 (4-((tert-butyldimethylsilyl)oxy)phenyl)methanol 
• 120743-99-9 p-[(tert-butyldimethylsilyl)oxy]benzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 540-38-5 p-Iodophenol 
• 197770-48-2 4-((4-fluorophenyl)ethynyl)phenol 
• 39769-24-9 (E)-4-fluoro-4'-methoxystilbene 
• 1145-93-3 diethyl 4-methoxybenzylphosphonate 
• 848487-62-7 (E)-1-methoxymethyloxy-4-(4-fluoro)styrylbenzene 
• 459-46-1 4-Fluorobenzyl bromide 
• 63909-58-0 diethyl (4-fluorobenzyl)phosphonate 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 

Downstream Products

• 137372-64-6 4-<2-(4-fluorophenyl)ethyl>phenol 
• 136922-49-1 4-Ethoxy-4'-fluor-trans-stilben 
• 39769-24-9 (E)-4-fluoro-4'-methoxystilbene 
• 1588534-23-9 C₂₈H₂₀F₂O₂ 
• 39769-08-9 N-(4-fluorobenzylidene)-4-methoxyaniline 
• 3230-50-0 4-(4-hydroxyphenyl)-N-(4-methoxyphenyl)imine 

Relevant articles and documents

Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage

C=C bond breaking to access the C=N bond remains an underdeveloped area. A new protocol for C=C bond cleavage of alkenes under nonoxidative conditions to produce imines via an iron-catalyzed nitrene transfer reaction of 4-hydroxystilbenes with aryl azides is reported. The success of various sequential one-pot reactions reveals that the good compatibility of this method makes it very attractive for synthetic applications. On the basis of experimental observations, a plausible reaction mechanism is also proposed.

Resveratrol derivative containing fluorine group, and preparation method and application

The invention belongs to the technical field of medicines and discloses a resveratrol derivative containing a fluorine group, and a preparation method and an application. The resveratrol derivative has the structural characteristics as shown in a general

NOVEL NUCLEOSIDE PHOSPHORAMIDATE COMPOUND AND USE THEREOF

The present invention provides a novel nucleoside phosphoramidate compound, or a stereoisomer, salt, hydrate, solvate or crystal thereof for the treatment of Flaviviridae family viral infection, especially hepatitis C viral infection. The present invention also provides the pharmaceutical composition comprising a compound of the present invention, or a stereoisomer, salt, hydrate, solvate or crystal thereof and a use of the compound or the composition of the present invention in the treatment of Flaviviridae family viral infection, especially hepatitis C viral infection. The compound of the present invention has a good anti-HCV effect.