156483-02-2

Upstream product

• 156558-16-6 methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate 
• 697-82-5 2,3,5-trimethylphenol 
• 4885-02-3 Dichloromethyl methyl ether 
• 156482-91-6 methyl (R)-7-(4-fluorophenyl)-7-(2-hydroxy-3,4,6-trimethylphenyl)heptanoate 

Downstream Products

• 156558-09-7 methyl (R)-7-(4-fluorophenyl)-7-(3-formyl-6-methoxy-2,4,5-trimethylphenyl)heptanoate 
• 156558-08-6 (R)-7-(4-fluorophenyl)-7-(3-formyl-6-hydroxy-2,4,5-trimethylphenyl)heptanoic acid 

Relevant academic research and scientific papers

Stereoselective synthesis and thromboxane A2 (TXA2) receptor antagonistic activity of optically active phenol derivatives

Enantiomers of four potent nonprostanoid thromboxane A2 (TXA2) receptor antagonists, (±)-7-(4-fluorophenyl)-7-(2-hydroxyphenyl)heptanoic acids (1- 4), were synthesized stereoselectively by direct ortho-alkylation of phenols under mod

Optically active phenol derivatives and preparation thereof

An optically active tri-substituted methane compound having, as substituents, an aromatic ring group and a phenyl group having hydroxyl group at ortho or para position can be obtained by allowing a phenol compound unsubstituted at the ortho- or/and para-p