848492-86-4

Basic information

• Product Name: Benzene, 4-methoxy-2-nitro-1-(2-propenyl)-
• CAS NO: 848492-86-4
• Molecular Formula: C10H11NO3
• Molecular Weight: 193.202
• Mol File: 848492-86-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 4-methoxy-2-nitro-1-(2-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 4-methoxy-2-nitro-1-(2-propenyl)-(848492-86-4)
• EPA Substance Registry System: Benzene, 4-methoxy-2-nitro-1-(2-propenyl)-(848492-86-4)

Safety Data

• Hazardous Substances Data: 848492-86-4(Hazardous Substances Data)

Upstream product

• 140-67-0 Estragole 
• 58755-70-7 1-iodo-4-methoxy-2-nitrobenzene 
• 106-95-6 allyl bromide 
• 33844-21-2 2-nitro-4-methoxybenzoic acid 
• 24850-33-7 allyltributylstanane 
• 10298-80-3 2-chloro-5-methoxynitrobenzene 
• 96-96-8 4-methoxy-2-nitroaniline 
• 5344-78-5 4-bromo-3-nitroanizole 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1050514-13-0 3-(4-methoxy-2-nitrophenyl)propan-1,2-diol 
• 59816-85-2 2-allyl-5-methoxy-phenylamine 
• 1050514-14-1 4-(4-methoxy-2-nitrobenzyl)-2,2-dimethyl-1,3-dioxolane 

Relevant articles and documents

PESTICIDAL COMPOSITIONS AND METHODS

This disclosure relates to the field of molecules having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the structure of Formula A.

Palladium(0)-catalyzed intramolecular decarboxylative allylation of ortho nitrobenzoic esters

A Pd/Ag bimetallic system has been developed for the decarboxylative allylation of ortho-nitrobenzoic esters in an intramolecular fashion. In contrast to the typical sp2-sp3 cross-coupling approach which requires air and moisture sensitive preformed organometallic reagents, we provide an alternative route to the synthesis of ortho-allyl nitroarenes from the corresponding ortho-nitrobenzoic acid derivatives. The reaction proceeds through a mechanistically distinct decarboxylative metalation pathway. A cooperative reactivity of palladium and silver is crucial for the reaction outcome.

QUINOXALINE COMPOUNDS AND USE THEREOF

The present invention is related to quinoxaline compounds of Formula (I) in particular for the treatment of autoimmune disorders and/or inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, bacterial or viral infections, kidney diseases, platelet aggregation, cancer, transplantation, graft rejection or lung injuries.