81574-51-8

Upstream product

• 81574-50-7 2,4-Dimethoxy-3-methyl-benzaldehyde oxime 
• 506-68-3 bromocyane 
• 5673-07-4 2,6-dimethoxytoluene 
• 7149-92-0 2,4-dimethoxy-3-methylbenzaldehyde 

Downstream Products

• 81574-49-4 2,4-dimethoxy-3-methylbenzoic acid 
• 74628-39-0 methyl 2,4-dimethoxy-6-(2,4,6-trimethoxy-3-methylphenoxy)-3-methylbenzoate 
• 74628-38-9 methyl 2,4-dimethoxy-6-(2,4,6-trimethoxyphenoxy)-3-methylbenzoate 
• 81574-61-0 methyl 6-(4-hydroxy-2,6-dimethoxy-3-methylphenoxy)-2,4-dimethoxy-3-methylbenzoate 
• 81574-64-3 methyl 6-(4-hydroxy-2,6-dimethoxyphenoxy)-2,4-dimethoxy-3-methylbenzoate 
• 81574-63-2 6-(4-hydroxy-2,6-dimethoxyphenoxy)-2,4-dimethoxy-3-methylbenzoic acid 
• 81574-66-5 4',6-dihydroxy-2,2',4,6'-tetramethoxy-3-methylbenzophenone 
• 81574-53-0 methyl 2-hydroxy-4-methoxy-3-methyl-5-nitrobenzoate 
• 81574-52-9 methyl 2,4-dimethoxy-3-methyl-5-nitrobenzoate 
• 81574-55-2 3-Amino-2-bromo-4,6-dimethoxy-5-methyl-benzoic acid methyl ester 
• 81574-57-4 methyl 5-bromo-2,4-dimethoxy-3-methylbenzoate 
• 81574-54-1 methyl 5-amino-2,4-dimethoxy-3-methylbenzoate 
• 81574-56-3 methyl 6-bromo-2,4-dimethoxy-3-methylbenzoate 
• 6688-71-7 methyl 2,4-dimethoxy-3-methylbenzoate 

Relevant academic research and scientific papers

Practical synthesis of aromatic nitriles via gallium-catalysed electrophilic cyanation of aromatic C-H bonds

A gallium-catalysed, direct cyanation reaction of aromatic and heteroaromatic C-H bonds with cyanogen bromide was developed as a practical synthetic method for the preparation of aromatic nitriles. The Royal Society of Chemistry 2012.

1,2,4-oxadiazolyl-phenoxyalkylisoxazoles and their use as antiviral agents

Compounds of the formula STR1 wherein: Y is alkylene of 3 to 9 carbon atoms; R1 is lower-alkyl, lower-alkoxy-(C1-3 -alkyl), lower-alkoxycarbonyl, cyclopropyl or trifluoromethyl; R2 and R3 independently are hydro

Depsidone Synthesis. Part 21. A New Synthesis of Grisa-2',5'-diene-3,4'-diones

Treatment of suitably substituted methyl 2-phenoxybenzoates with titanium(IV) chloride and dry hydrogen chloride afforded grisa-2',5'-diene-3,4'-diones in high yield.The structures of these compounds followed from their thermal stability, their methanolysis to methyl 2-(4-hydroxyphenoxy)benzoates, and their reductive cleavage to 2,4'-dihydrobenzophenones.Treatment of the benzophenones with base gave xanthones.An attempt to synthesize dehydrogriseofulvin (1) by this method failed.