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17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate

Base Information Edit
  • Chemical Name:17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate
  • CAS No.:95498-58-1
  • Molecular Formula:C37H54ClIO4
  • Molecular Weight:725.191
  • Hs Code.:
  • Mol file:95498-58-1.mol
17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate

Synonyms:17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate Edit
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Technology Process of 17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate

There total 6 articles about 17-chloro-5α-cholestane-3β,5-diol 3-acetate 5-(4-iodophenyl)acetate 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 sulfuryl dichloride; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at -10 ℃; for 2.5h; Irradiation;
DOI:10.1016/S0040-4020(01)82345-0
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) O2, 2.) H2 / 2.) PtO2*H2O / 1.) CH2Cl2/pyridine, irradiation, 14 h, 15 deg C, 2.) ethyl acetate, room temperature, atmospheric pressure, 10 h
2: 74 percent / calcium hydride, tetra-n-butylammonium iodide / toluene / Heating
3: 59 percent / azobis(isobutyronitrile), SO2Cl2 / CCl4 / 2.5 h / -10 °C / Irradiation
With sulfuryl dichloride; calcium hydride; 2,2'-azobis(isobutyronitrile); hydrogen; oxygen; tetra-(n-butyl)ammonium iodide; platinum(IV) oxide; In tetrachloromethane; toluene;
DOI:10.1016/S0040-4020(01)82345-0
Guidance literature:
Multi-step reaction with 4 steps
1: pyridine
2: 1.) O2, 2.) H2 / 2.) PtO2*H2O / 1.) CH2Cl2/pyridine, irradiation, 14 h, 15 deg C, 2.) ethyl acetate, room temperature, atmospheric pressure, 10 h
3: 74 percent / calcium hydride, tetra-n-butylammonium iodide / toluene / Heating
4: 59 percent / azobis(isobutyronitrile), SO2Cl2 / CCl4 / 2.5 h / -10 °C / Irradiation
With pyridine; sulfuryl dichloride; calcium hydride; 2,2'-azobis(isobutyronitrile); hydrogen; oxygen; tetra-(n-butyl)ammonium iodide; platinum(IV) oxide; In tetrachloromethane; toluene;
DOI:10.1016/S0040-4020(01)82345-0
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