113748-80-4

Downstream Products

• 113748-81-5 3-methoxy-6,7-dihydro-8-bromo-9-<4-<2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenoxy>phenyl>-5H-benzocycloheptene 
• 109610-82-4 3-methoxy-6,7-dihydro-8-phenyl-9-(4-hydroxyphenyl)-5H-benzocycloheptene 
• 113748-77-9 6,7-dihydro-8-phenyl-9-<4-<2-(dimethylamino)ethoxy>phenyl>-5H-benzocyclohepten-3-ol 
• 113748-79-1 3-<2-(dimethylamino)ethoxy>-6,7-dihydro-8-phenyl-9-(hydroxyphenyl)-5H-benzocycloheptene 
• 113748-83-7 3-methoxy-6,7-dihydro-8-phenyl-9-<4-<2-(dimethylamino)ethoxy>phenyl>-5H-benzocycloheptene 
• 113748-84-8 6,7-dihydro-8-phenyl-9-<4-<2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenoxy>phenyl>-5H-benzocyclohepten-3-ol 
• 113748-82-6 3-methoxy-6,7-dihydro-8-phenyl-9-<4-<2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenoxy>phenyl>-5H-benzocycloheptene 
• 113748-85-9 3-(2-chloroethoxy)-6,7-dihydro-8-phenyl-9-<4-<2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenoxy>phenyl>-5H-benzocycloheptene 

Relevant academic research and scientific papers

Nonisomerizable Analogues of (Z)- and (E)-4-Hydroxytamoxifen. Synthesis and Endocrinological Properties of Substituted Diphenylbenzocycloheptenes

Substituted 8,9-diphenyl-6,7-dihydro-5H-benzocycloheptenes 6-8, which are ring-fused analogues of (Z)-trans-4-hydroxytamoxifen, (E)-cis-tamoxifen, and (E)-cis-4-hydroxytamoxifen, were synthesized from 7-methoxy-1-benzosuberone.The hydroxy compounds 6 and