94909-58-7

Upstream product

• 96835-38-0 Bis-(4-methoxy-phenyl)-(1-methyl-[4]piperidyl)-methanol 
• 1570-45-2 isonicotinic acid ethylester 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 1690-75-1 1-methyl-piperidine-4-carboxylic acid methyl ester 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 50-00-0 formaldehyd 
• 133365-39-6 methyl 4-[(4-methoxyphenyl)(piperidin-4-ylidene)methyl]phenoxide 
• 29976-53-2 N-ethoxycarbonyl-4-piperidone 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 96835-35-7 4-[Hydroxy-bis-(4-methoxy-phenyl)-methyl]-1-methyl-pyridinium; iodide 
• 67916-57-8 bis(4-methoxyphenyl)-4-pyridylmethanol 

Downstream Products

• 96835-43-7 Acetic acid 4-[(4-acetoxy-phenyl)-(1-methyl-piperidin-4-ylidene)-methyl]-phenyl ester 

Relevant academic research and scientific papers

Symmetric 4,4′-(piperidin-4-ylidenemethylene)bisphenol derivatives as novel tunable estrogen receptor (ER) modulators

We designed and synthesized 4,4′-(piperidin-4-ylidenemethylene)bisphenol derivatives as novel tunable estrogen receptor (ER) modulators. The introduction of hydrophobic substituents on the nitrogen atom of the piperidine ring enhanced ERα binding affinity

Antiimplantation Agents: Part IV - 4-Benzhydrylidenepiperidines and Tetrahydropyran Analogues of F 6066

Several α-(4-pyridyl)enzhydrols (8) have been synthesised by Grignard reaction on 4-aroylpyridines (6) or ethyl isonicotinate (7).The quaternary salts 9 of 8 are reduced catalytically to α-(4-piperidyl)benzhydrols (10) which undergo dehydration to benzhyd