24705-61-1

Upstream product

• 18978-24-0 meso-3,4-bis-(4-hydroxy-phenyl)-hexane-3,4-diol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 7507-01-9 racem.-3.4-bis-(4-hydroxy-phenyl)-hexanediol-(3.4) 
• 64-17-5 ethanol 
• 74063-42-6 3,4-bis-(4-acetoxy-phenyl)-3,4-dibromo-hexane 
• 25743-56-0 4-(1-oxopropyl)phenyl acetate 
• 13029-44-2 dienestrol 
• 7507-01-9 3,4-bis(4-hydroxyphenyl)-3,4-hexanediol 
• 110-86-1 pyridine 

Downstream Products

• 24643-94-5 6-acetoxy-2-(4-acetoxy-phenyl)-3-ethyl-1-methyl-indene 
• 70101-27-8 C₁₉H₂₀O₃ 
• 70101-28-9 Ω-hydroxydienestrol 
• 35495-11-5 Z,Z-dienestrol 
• 84-16-2 hexestrol 
• 71855-45-3 indanestrol 
• 6033-96-1 3.4-bis-(4-propionyloxy-phenyl)-hexadiene-(2t.4t) 
• 38028-29-4 5-acetoxy-2-(4-acetoxy-phenyl)-1-ethyl-3-methyl-indene 
• 38028-27-2 1-ethyl-2-(4-hydroxyphenyl)-3-methylinden-5-ol 
• 82699-02-3 2,3,4,5-Bisepoxy-3,4-bis(4'-acetoxyphenyl)-hexan 
• 5965-06-0 trans-<4,4'-(diethylvinylen) bis (phenyl)>diacetate 
• 82699-01-2 2,3-Epoxy-3,4-bis(4'-acetoxyphenyl)-E,E-hexen-4 
• 102460-41-3 optically inactive 3,4-bis-(4-acetoxy-phenyl)-2,5-dibromo-hex-3t-ene 
• 13029-44-2 dienestrol 

Relevant academic research and scientific papers

Configuration of dienestrol

Uncertainty concerning the configuration of dienestrol was resolved by a detailed spectrochemical investigation, including single crystal X ray diffraction, of the active drug and its stereoisomers. A symmetric structure in which the phenyl and methyl groups are cis about each double bond is unambiguously assigned.