342898-65-1

Basic information

• Product Name: 11α-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene-11β-ol
• Synonyms: 11α-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene-11β-ol
• CAS NO: 342898-65-1
• Molecular Weight: 508.701
• Mol File: 342898-65-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 11α-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene-11β-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 11α-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene-11β-ol(342898-65-1)
• EPA Substance Registry System: 11α-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene-11β-ol(342898-65-1)

Safety Data

• Hazardous Substances Data: 342898-65-1(Hazardous Substances Data)

Upstream product

• 89155-71-5 (8S,9S,13S,14S,17S)-3,17-bis(benzyloxy)-13-methyl-6,7,8,9,12,13,14,15,16,17-decahydro-11H-cyclopenta[a]phenanthren-11-one 
• 1730-25-2 allylmagnesium bromide 
• 40128-86-7 3,17β-Bis(benzyloxy)estra-1,3,5(10),9(11)-tetraene 
• 40128-87-8 11α-hydroxy-3,17β-dibenzyloxyoestra-1,3,5(10)-triene 
• 69455-04-5 3,17β-bis(benzyloxy)estra-1,3,5(10)-triene 
• 100-39-0 benzyl bromide 
• 50-28-2 estradiol 

Downstream Products

• 1599458-17-9 C₄₁H₅₄O₃Si 
• 1373112-28-7 3-t-butyldiphenylsiloxy-11β-(3-isopropoxypropyl)estra-1,3,5(10)-trien-17-one 
• 1599458-16-8 C₄₁H₅₆O₃Si 
• 1373112-27-6 3-t-butyldiphenylsilyloxy-11β-(3-isopropoxypropyl)estra-1,3,5(10)-trien-17β-ol 
• 849241-77-6 3,17β-dibenzyloxy-11β-(3-tert-butoxypropyl)estra-1,3,5(10)-triene 
• 849241-76-5 3,17β-dibenzyloxy-11β-(3-isopropoxypropyl)estra-1,3,5(10)-triene 
• 849241-75-4 3-(3,17β-dibenzyloxyestra-1,3,5(10)-trien-11β-yl)propyl toluenesulfonate 
• 534572-63-9 3-(3,17β-dibenzyloxyestra-1,3,5(10)-trien-11β-yl)propanoic acid 
• 147250-16-6 3,17β-dibenzyloxy-11β-(3'-hydroxypropyl)estra-1,3,5(10)-triene 
• 534572-62-8 11β-allyl-3,17β-dibenzyloxyestra-1,3,5(10)-triene 
• 342898-89-9 3,17β-bis(benzyloxy)-11-(2-propenyl)estra-1,3,5(10),9(11)-tetraene 

Relevant articles and documents

Synthesis of 11β-ether-17α-ethinyl-3,17β-estradiols with strong ER antagonist activities

We have previously found that several families of nonpolar short chain 11β-ethers and esters of estradiol are selective estrogen receptor modulators (SERMs). Surprisingly, the transformation from potent estrogen to anti-estrogen occurs when the 11β-side c

Synthesis and evaluation of B-, C-, and D-ring-substituted estradiol carboxylic acid esters as locally active estrogens

We have synthesized derivatives of estradiol that are structurally modified to serve as "soft" estrogens and act within a geographically limited area of the body; estrogens without systemic action. We have previously shown with 16α-substituted analogues o