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rac Enterodiol-d6

Base Information
  • Chemical Name:rac Enterodiol-d6
  • CAS No.:104411-12-3
  • Molecular Formula:C18H22O4
  • Molecular Weight:308.323
  • Hs Code.:
rac Enterodiol-d6

Synonyms:

Suppliers and Price of rac Enterodiol-d6
Supply Marketing:
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
  • Usbiological
  • rac Enterodiol-d6
  • 1mg
  • $ 885.00
  • TRC
  • racEnterodiol-d6
  • 10mg
  • $ 4540.00
  • Medical Isotopes, Inc.
  • racEnterodiol-d6
  • 25 mg
  • $ 6750.00
  • Medical Isotopes, Inc.
  • racEnterodiol-d6
  • 10 mg
  • $ 4750.00
  • Medical Isotopes, Inc.
  • racEnterodiol-d6
  • 1 mg
  • $ 950.00
Total 3 raw suppliers
Chemical Property of rac Enterodiol-d6
Chemical Property:
  • Melting Point:176-178oC 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Methanol (Slightly) 
Purity/Quality:

>98% *data from raw suppliers

rac Enterodiol-d6 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Isotope labelled rac Enterodiol, a compound closely related to Enterolactone (E558950). A metabolite of sesame lignans (sesamin, sesamolin). Inhibits colonic cancer cell growth by inducing cell cycle arrest and apoptosis. Possible relationship between exposure and reduced risk of breast cancer.
Technology Process of rac Enterodiol-d6

There total 2 articles about rac Enterodiol-d6 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 lithium aluminium tetrahydride;
Guidance literature:
Multi-step reaction with 2 steps
1: 0.23 g / D2O, PBr3 / 5 h / Heating
2: LiAlH4
With lithium aluminium tetrahydride; water-d2; phosphorus tribromide;
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