129835-67-2

Upstream product

• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 134868-93-2 3-(benzyloxy)-5-(hydroxymethyl)phenol 

Downstream Products

• 134868-75-0 4-(3-Benzyloxy-5-formyl-phenoxymethyl)-benzoic acid methyl ester 
• 134868-74-9 3-Benzyloxy-5-(4-bromo-benzyloxy)-benzaldehyde 
• 129835-68-3 4-(3-Benzyloxy-5-formyl-phenoxymethyl)-benzonitrile 
• 1010413-01-0 3-(benzyloxy)-5-formylphenyl trifluoromethanesulfonate 
• 134868-78-3 1-Benzyloxy-3-(4-bromo-benzyloxy)-5-bromomethyl-benzene 
• 134868-76-1 [3-Benzyloxy-5-(4-bromo-benzyloxy)-phenyl]-methanol 
• 129835-69-4 4-(3-Benzyloxy-5-hydroxymethyl-phenoxymethyl)-benzonitrile 
• 129835-70-7 4-(3-Benzyloxy-5-bromomethyl-phenoxymethyl)-benzonitrile 
• 134868-79-4 4-(3-Benzyloxy-5-bromomethyl-phenoxymethyl)-benzoic acid methyl ester 
• 134868-77-2 4-(3-Benzyloxy-5-hydroxymethyl-phenoxymethyl)-benzoic acid methyl ester 
• 134868-81-8 4-{3-Benzyloxy-5-[3-(3,5-bis-benzyloxy-benzyloxy)-5-bromomethyl-phenoxymethyl]-phenoxymethyl}-benzonitrile 
• 134868-80-7 4-{3-Benzyloxy-5-[3-(3,5-bis-benzyloxy-benzyloxy)-5-hydroxymethyl-phenoxymethyl]-phenoxymethyl}-benzonitrile 

Relevant academic research and scientific papers

1H-INDOLE-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS PPAR MODULATORS

The present invention relates to certain indole derivatives that are modulators of PPAR, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.

Antibacterial macrocycles with substituted biphenyl

The invention relates to antibacterial macrocycles with substituted biphenyl and processes for their preparation, their use for the treatment and/or prophylaxis of diseases, and their use for the production of medicaments for the treatment and/or prophylaxis of diseases, especially of bacterial infections.

Polymers with Controlled Molecular Architecture: Control of Surface Functionality in the Synthesis of Dendritic Hyperbranched Macromolecules using the Convergent Approach

The synthesis of unsymmetrically or non-uniformly surface-functionalized dentritic macromolecules using a stepwise convergent-growth approach is described.By stepwise alkylation of the monomer unit, 3,5-dihydroxybenzyl alcohol, with unsubstituted and subs