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10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat

Base Information Edit
  • Chemical Name:10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat
  • CAS No.:13236-11-8
  • Molecular Formula:C22H28O5
  • Molecular Weight:372.461
  • Hs Code.:
  • Mol file:13236-11-8.mol
10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ<sup>4</sup>-oestren-3-on-17β-acetat

Synonyms:

Suppliers and Price of 10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 10β-HydroperoxyNorethindroneAcetate
  • 10mg
  • $ 1185.00
  • TRC
  • 10β-HydroperoxyNorethindroneAcetate
  • 5mg
  • $ 635.00
  • TRC
  • 10β-HydroperoxyNorethindroneAcetate
  • 2.5mg
  • $ 360.00
  • TRC
  • 10β-HydroperoxyNorethindroneAcetate
  • 1mg
  • $ 165.00
Total 5 raw suppliers
Chemical Property of 10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat Edit
Chemical Property:
  • Melting Point:178-180 °C 
  • Boiling Point:513.2±50.0 °C(Predicted) 
  • Density:1.24±0.1 g/cm3(Predicted) 
Purity/Quality:

95%+ or 98%+ *data from raw suppliers

10β-HydroperoxyNorethindroneAcetate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 10β-Hydroperoxy Norethindrone Acetate is a derivative of Norethindrone (N676000), a progesterone in combination with acetate used as an oral contraceptive (1,2). It is reasonably anticipated to be a human carcinogen.
Technology Process of 10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat

There total 3 articles about 10β-Hydroperoxy-17α-ethinyl-17β-hydroxy-Δ4-oestren-3-on-17β-acetat 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:
17α-Ethinyl-17β-hydroxy-Δ5(10)-oestren-3-on-17β-acetat, O2, Bestrahlung;
DOI:10.1021/jo01268a090
Guidance literature:
Acetat II, O2, photochemisch;
Guidance literature:
Estren III, hν/O2;
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