69194-92-9

Upstream product

• 55687-94-0 4-(1-hydroxy-1-methylethyl)-3,5-dimethoxybenzaldehyde 
• 140464-79-5 methyl 2,6-dimethoxy-4-dimethoxymethylbenzoate 
• 59276-37-8 3,4,5-trimethoxybenzaldehyde dimethyl acetal 
• 55687-80-4 methyl 2,6-dimethoxy-4-(α,α-diethoxymethyl)benzoate 
• 16849-68-6 dimethyl 2,6-dimethoxyterephthalate 
• 33187-98-3 3,5-dimethoxy-4-(methoxycarbonyl)benzaldehyde 

Downstream Products

• 69194-94-1 4-isopropenyl-3,5-dimethoxy-α-(morpholinomethylene)-dihydrocinnamic acid nitrile 
• 69195-05-7 α-(aminomethylene)-3,5-dimethoxy-4-isopropenylhydrocinnamic acid nitrile 
• 74731-66-1 5-(4-Isopropyl-3,5-dimethoxy-benzyl)-pyrimidine-2,4-diamine 
• 69194-95-2 (Z)-2-(4-Isopropenyl-3,5-dimethoxy-benzyl)-3-phenylamino-acrylonitrile 
• 69194-91-8 2,4-diamino-5-(4-isopropenyl-3,5-dimethoxybenzyl)-pyrimidine 
• 566934-92-7 5-dimethoxymethyl-2-isopropenyl-1,3-dimethoxy-benzene 
• 344396-19-6 3,5-dimethoxy-4-(1-methylethyl)benzaldehyde 
• 141509-20-8 (E)-1,3-dimethoxy-2-(1-methylethyl)-5-(2-phenylethenyl)benzene 

Relevant academic research and scientific papers

Synthesis of antibiotic stilbenes by reductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal

Reductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal followed by reaction with suitable electrophiles is the key step of a reaction sequence leading to the synthesis of naturally occurring 4-alkyl-3,5-dihydroxy-substituted trans-stilbenes

Synthesis and antimicrobial activity of C(4')-substituted analogs of trimethoprim

A series of 2,4-diamino-5-(3,5-dimethoxybenzyl)-pyrimidines substitute at C(4') of the benzene ring with a functionalized carbon atom was synthesized. The target substances were tested for inhibition of dihydrofolate reductases from E. coli and rat liver,

Benzylpyrimidine derivatives

Benzylpyrimidines of the formula STR1 wherein R1 and R2, independently, are C1-6 -alkyl, R3 is C1-3 -alkyl and R4 is methylene or C2-4 -alkylidene and physiologically compatible