1335093-90-7

Basic information

• Product Name: (E)-1-(2-fluoroethoxy)-2-methoxy-4-(2-nitrovinyl)benzene
• Synonyms: (E)-1-(2-fluoroethoxy)-2-methoxy-4-(2-nitrovinyl)benzene
• CAS NO: 1335093-90-7
• Molecular Weight: 241.219
• Mol File: 1335093-90-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-fluoroethoxy)-2-methoxy-4-(2-nitrovinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-fluoroethoxy)-2-methoxy-4-(2-nitrovinyl)benzene(1335093-90-7)
• EPA Substance Registry System: (E)-1-(2-fluoroethoxy)-2-methoxy-4-(2-nitrovinyl)benzene(1335093-90-7)

Safety Data

• Hazardous Substances Data: 1335093-90-7(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 914394-64-2 4-(2-fluoroethoxy)-3-methoxybenzaldehyde 
• 75-52-5 nitromethane 

Downstream Products

• 1335093-92-9 1-(2-fluoroethoxy)-2-methoxy-4-(1-methoxy-2-nitroethyl)benzene 
• 1335093-52-1 7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline 
• 1335093-44-1 1-(5-bromo-2-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-49-6 1-(4-fluoro-3-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-48-5 1-(3,5-dimethoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-47-4 7-(2-fluoroethoxy)-1-(3-(2-fluoroethoxy)-4-methoxybenzyl)-6-methoxyisoquinoline 
• 1335093-46-3 1-(3-fluorobenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-45-2 1-(3-bromo-4-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-43-0 1-(2-fluoro-4-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-42-9 7-(2-fluoroethoxy)-6-methoxy-1-(4-(methylthio)benzyl)isoquinoline 
• 1335093-41-8 7-(2-fluoroethoxy)-6-methoxy-1-(4-methoxy-3-methylbenzyl)-isoquinoline 
• 1335093-94-1 2-(4-(2-fluoroethoxy)-3-methoxyphenyl)-2-methoxyethanamine 
• 1335093-40-7 1-(4-fluoro-3-methoxybenzyl)-7-(2-fluoroethoxy)-6-methoxyisoquinoline 
• 1335093-68-9 7-(2-fluoroethoxy)-1-(4-(2-fluoroethoxy)-3-methoxybenzyl)-6-methoxyisoquinoline oxalate 

Relevant articles and documents

Synthesis and in vitro evaluation of new analogues as inhibitors for phosphodiesterase 10A

A series of analogues were synthesized by optimizing the structure of papaverine. The in vitro PDE10A binding affinity (IC50) values for these new analogues were measured; for compounds that have IC50 value less than 60 nM for PDE10A