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(Z)-Fluorotamoxifen

Base Information
  • Chemical Name:(Z)-Fluorotamoxifen
  • CAS No.:77588-48-8
  • Molecular Formula:C26H28FNO
  • Molecular Weight:389.513
  • Hs Code.:
(Z)-Fluorotamoxifen

Synonyms:(Z)-Fluorotamoxifen

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Chemical Property of (Z)-Fluorotamoxifen
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Technology Process of (Z)-Fluorotamoxifen

There total 11 articles about (Z)-Fluorotamoxifen which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogen fluoride; In benzene; Title compound not separated from byproducts; 1.) RT, 0.5 h, 2.) 50 deg C, 10 min;
DOI:10.1021/jm00148a022
Guidance literature:
Multi-step reaction with 4 steps
1: 75 percent / AlCl3 / CS2 / 1 h / Ambient temperature
2: 1.) Mg / 2.) ether, 2.) ether, reflux, 4 h
3: 85 percent / BBr3 / CH2Cl2 / 1 h / Ambient temperature
4: KOH / ethanol / 20 h / Heating
With potassium hydroxide; aluminium trichloride; boron tribromide; magnesium; In carbon disulfide; ethanol; dichloromethane;
DOI:10.1021/jm00148a022
Guidance literature:
Multi-step reaction with 6 steps
1: 62 percent / Na2S2O4*H2O / ethanol / Heating
2: 1.) conc. aq. HCl, NaNO2 / 1.) H2O, 20 min, 2.) H2O, RT, 0.5 h
3: 37 percent / 40percent aq. HF / benzene / 1.) RT, 0.5 h, 2.) 50 deg C, 10 min
4: 1.) Mg / 2.) ether, 2.) ether, reflux, 4 h
5: 85 percent / BBr3 / CH2Cl2 / 1 h / Ambient temperature
6: KOH / ethanol / 20 h / Heating
With hydrogenchloride; potassium hydroxide; sodium dithionite; hydrogen fluoride; boron tribromide; magnesium; sodium nitrite; In ethanol; dichloromethane; benzene;
DOI:10.1021/jm00148a022
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