53544-07-3

Upstream product

• 222622-96-0 5-(benzyloxy)-1-bromo-2-(bromomethyl)-4-methoxybenzene 
• 348618-45-1 3-(4-benzyloxy-2-bromo-5-methoxyphenyl)propionitrile 

Downstream Products

• 348618-46-2 4-Benzyloxy-7-(4-chloro-phenylsulfanyl)-3-methoxybicyclo [4.2.0]octa-1,3,5-triene-7-carbonitrile 
• 629652-75-1 4-benzyloxy-3-methoxy-7-methylsulfanyl-bicyclo[4.2.0]octa-1⁽⁶⁾,2,4-triene-7-carbonitrile 
• 348618-47-3 4-benzyloxy-3-methoxy-7-phenylsulfanylbicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile 
• 141039-11-4 4-benzyloxy-7-<(3,5-dibenzyloxyphenyl)oxy>methyl-7-carboxyl-3-methoxybicyclo<4.2.0>octa-1,3,5-triene 
• 141039-10-3 4-benzyloxy-7-<(3,5-dibenzyloxyphenyl)oxy>methyl-7-cyano-3-methoxybicyclo<4.2.0>octa-1,3,5-triene 
• 141039-12-5 tribenzylmuscomosin 

Relevant academic research and scientific papers

Regioselective synthesis of a potent Src kinase inhibitor: 4-(2,4-Dichloro-5-methoxyphenylamino)-7-methoxy-8-(2-morpholin-4-ylethoxy) benzo[g]quinoline-3-carbonitrile

The regioselective synthesis of compound 3, a potent Src kinase inhibitor is described. A key step in this synthesis is the regioselective thermal rearrangement of a substituted benzocyclobutene to provide a 2,3,6,7-tetrasubstituted naphthalene. An effici

Method for the regioselective preparation of substituted benzo[g]quinoline3-carbonitriles and benzo[g]quinazolines

This invention relates to a method for the regioselective synthesis of 4,6,7,8-substituted benzo[g]quinoline-3-carbonitriles and 4,6,7,8-substituted benzo[g]quinazolines as well as intermediates thereof. The compounds derived from this invention are usefu

Tricyclic protein kinase inhibitors

This invention provides compounds of formula 1, having the structure which are useful as inhibitors of protein tyro sine kinase and are antiproliferative agents.