81267-58-5

Upstream product

• 156-38-7 4-hydroxyphenylacetate 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 157519-74-9 5-(4-Hydroxyphenyl)-2-(4-n-octyloxycyclphexyl)pyrimidine 
• 118808-35-8 5-(4-hydroxyphenyl)-2-octylpyrimidine 
• 81267-53-0 4',5,7-trihydroxyisoflavylium chloride 
• 81267-70-1 cis-2,3-4',5,7-triacetoxy-2-methoxyisoflavan 
• 65998-43-8 4',5,7-triacetoxyisoflavan 
• 81267-64-3 4',5,7-triacetoxyisoflav-3-ene 
• 81267-63-2 isoflav-3-ene-4',5,7-triol 
• 201489-53-4 (4-dec-9-enyloxy)phenyl malonaldehyde 
• 945376-95-4 4-(3-bromopyrazolo[1,5-a]pyrimidin-6-yl)phenol 
• 137225-56-0 5-[4-((S)-3,7-Dimethyl-oct-6-enyloxy)-phenyl]-2-octyl-pyrimidine 
• 117814-30-9 2-Dodecyl-5-[4-((S)-6-methyl-octyloxy)-phenyl]-pyrimidine 
• 117814-50-3 2-Dodecyl-5-[4-((S)-4-methyl-hexyloxy)-phenyl]-pyrimidine 
• 137304-94-0 5-[4-((S)-3,7-Dimethyl-octyloxy)-phenyl]-2-octyl-pyrimidine 
• 117814-45-6 (S)-2-Octyl-5-<4-(6-methyloctyloxy)phenyl>pyrimidine 

Relevant academic research and scientific papers

TREATMENT OF ALZHEIMER'S DISEASE AND RELATED CONDITIONS

Compounds of formula (I) inhibit microtubule affinity regulating kinase (MARK), and hence are suitable for treating diseases associated with abnormal phosphorylation of tau.

Synthesis and Characterization of Copper(II) and Nickel(II) Complexes Derived from α-Substituted Malondialdehydes

The synthesis and characterization of two series of novel bis(4'-alkyloxyphenyl)malondialdehydes of copper(II) and nickel(II), (R=CnH2n+1, n = 9, 10, 11, 12) from 2-(4'-hydroxyphenyl)-3-dimethylamino acrolein is described. - Keywords

Synthesis and Mesomorphic Properties of Ferroelectric Liquid Crystals Bearing 5-Phenylpyrimidine Rings

Seventeen homologs of chiral 5-phenylpyrimidines were synthesized and their mesomorphic properties were evaluated with a DSC and a polarizing microscope.All compounds studied possessed an alkyl or alkoxy side chain at the p,p'-position of the 5-phenylpyri

A Synthesis of Hydroxylated Isoflavylium Salts and Their Reduction Products

Phloroglucinol reacts with arylmalondialdehydes in the presence of hydrochloric acid to form 5,7-dihydroxyisoflavylium salts.Reduction of these salts can be utilized to form isoflav-2-enes, isoflav-3-enes or isoflavans.