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7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene

Base Information Edit
  • Chemical Name:7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene
  • CAS No.:756844-33-4
  • Molecular Formula:C27H34O2S
  • Molecular Weight:422.632
  • Hs Code.:
  • Mol file:756844-33-4.mol
7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene

Synonyms:7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene

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Chemical Property of 7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene Edit
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Technology Process of 7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene

There total 5 articles about 7α-benzylthio-3,17β-bis(methoxy)estra-1,3,5(10)-triene 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 triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; at 0 ℃;
DOI:10.1016/j.bmc.2004.06.017
Guidance literature:
Multi-step reaction with 5 steps
1.1: t-BuOK; diisopropylamine; n-BuLi / tetrahydrofuran; hexane / 0.33 h / -15 °C
1.2: 80 percent / trimethylborate; H2O2 / H2O; tetrahydrofuran; hexane / 1 h / 20 °C
2.1: 100 percent / PCC / CH2Cl2 / 1 h / 20 °C
3.1: 100 percent / bromine / CH2Cl2; CCl4
4.1: 90 percent / NaOH; tetrabutylammonium hydrogensulfate / H2O; benzene / 2 h / 20 °C
5.1: 82 percent / boron trifluoride etherate; triethylsilane / CH2Cl2 / 0 °C
With triethylsilane; sodium hydroxide; n-butyllithium; boron trifluoride diethyl etherate; potassium tert-butylate; bromine; tetra(n-butyl)ammonium hydrogensulfate; diisopropylamine; pyridinium chlorochromate; In tetrahydrofuran; tetrachloromethane; hexane; dichloromethane; water; benzene;
DOI:10.1016/j.bmc.2004.06.017
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / bromine / CH2Cl2; CCl4
2: 90 percent / NaOH; tetrabutylammonium hydrogensulfate / H2O; benzene / 2 h / 20 °C
3: 82 percent / boron trifluoride etherate; triethylsilane / CH2Cl2 / 0 °C
With triethylsilane; sodium hydroxide; boron trifluoride diethyl etherate; bromine; tetra(n-butyl)ammonium hydrogensulfate; In tetrachloromethane; dichloromethane; water; benzene;
DOI:10.1016/j.bmc.2004.06.017
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