337535-27-0

Upstream product

• 108-36-1 1,3-dibromobenzene 
• 10365-98-7 3-methoxyphenylboronic acid 
• 108-86-1 bromobenzene 
• 1003858-50-1 2-(3-methoxyphenyl)-5, 5-dimethyl-1,3,2-dioxaborinane 
• 17878-47-6 (3-bromophenyl)trimethylsilane 

Downstream Products

• 1233720-86-9 2-(3'-methoxybiphenyl-3-yl)-1-benzothiophene 
• 1373123-17-1 3-(2-hydroxyadamantan-2-yl)-3'-hydroxybiphenyl 
• 1373123-40-0 (3'-methoxybiphenyl-3-yl)diphenylmethanol 
• 1373123-33-1 3-(2-hydroxyadamantan-2-yl)-3'-methoxybiphenyl 
• 1373123-19-3 (3'-hydroxybiphenyl-3-yl)diphenylmethanol 
• 1373123-35-3 C₂₂H₂₃⁽²⁾HO₂ 
• 1373123-36-4 C₂₂H₂₃⁽²⁾HO₂ 
• 1373123-26-2 3-[(2-hydroxyethylamino)diphenylmethyl]-3'-hydroxybiphenyl 
• 1373123-25-1 3-[(2,2,2-trifluoroethoxy)diphenylmethyl]-3'-hydroxybiphenyl 
• 1373123-23-9 3-[2-(2,2,2-trifluoroethoxy)adamantan-2-yl]-3'-hydroxybiphenyl 
• 1373123-41-1 3'-(methoxydiphenylmethyl)-3-hydroxybiphenyl 
• 1373123-34-2 3-(2-methoxyadamantan-2-yl)-3'-hydroxybiphenyl 

Relevant academic research and scientific papers

Visible-Light-Promoted, Catalyst-Free Gomberg-Bachmann Reaction: Synthesis of Biaryls

Biaryls were synthesized via a novel visible-light-promoted Gomberg-Bachmann reaction that does not require a photosensitizer or any metal reagents. The formation of an electron donor-acceptor complex between aryl diazonium salts and pyridine allows, under visible-light irradiation, the synthesis of biaryls in moderate-to-high yields.

Novel estrone mimetics with high 17β-HSD1 inhibitory activity

17β-Hydroxysteroid dehydrogenase type 1 (17β-HSD1) catalyzes the reduction of estrone into estradiol, which is the most potent estrogen in humans. Lowering intracellular estradiol concentration by inhibition of this enzyme is a promising new option for th

Controlled monoarylation of dibromoarenes in water with a polymeric palladium catalyst

A highly selective monoarylation of dibromoarenes was performed via the Suzuki-Miyaura cross-coupling with arylboronic acids with an amphiphilic polystyrene-poly(ethylene glycol) (PS-PEG) resin-supported phosphine-palladium complex in water under heteroge

1-substituted phenyl-1-(1h-imidazol-4-yl) alcohols, process for producing the same and use thereof

To provide a composition having a steroid C17,20-lyase inhibitory activity and useful as an agent for the prophylaxis or treatment of prostatism and tumors such as breast cancer. A compound represented by the formula: wherein R is a hydrogen atom or a protecting group, R1is a lower alkyl group or a cyclic hydrocarbon group, R2is an aromatic hydrocarbon group optionally having substituents or an aromatic heterocyclic group optionally having substituents, R3is a hydrocarbon group optionally having substituents, a hydroxyl group optionally having substituents, a thiol group optionally having substituents, an amino group optionally having substituents, an acyl group or a halogen atom, and n is an integer of 0 to 4, and a salt thereof have a steroid C17,20-lyase inhibitory activity, and are useful as an agent for the pophylaxis or treatment of prostatism and tumors such as beast cancer and the like.