Tetrahydronorethindrone

Base Information

Chemical Name:Tetrahydronorethindrone
CAS No.:25796-09-2
Molecular Formula:C₂₀H₃₀O₂
Molecular Weight:302.457
Hs Code.:
UNII:W5AMZ23GWD
ChEMBL ID:CHEMBL3273990
Nikkaji Number:J358.499B
Mol file:25796-09-2.mol

Synonyms:17-ethynyl-5-estrane-3,17-diol;17-ethynyl-5-estrane-3,17-diol, (17alpha)-isomer;17-ethynyl-5-estrane-3,17-diol, (3alpha,5alpha,17alpha)-isomer;17-ethynyl-5-estrane-3,17-diol, (3beta,5alpha,17alpha)-isomer;17-ethynyl-5-estrane-3,17-diol, (3beta,5beta,17alpha)-isomer;19-norpregn-20-yne-3,17-diol;tetrahydronorethindrone

Suppliers and Price of Tetrahydronorethindrone

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

Total 7 raw suppliers

Chemical Property of Tetrahydronorethindrone

Chemical Property:

Vapor Pressure:3.72E-09mmHg at 25°C
Melting Point:188-190°C
Boiling Point:428.9°Cat760mmHg
Flash Point:192.5°C
PSA：40.46000
Density:1.13g/cm³
LogP:3.36420
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly)
XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:302.224580195
Heavy Atom Count:22
Complexity:505

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12CCC3C4CCC(CC4CCC3C1CCC2(C#C)O)O
Isomeric SMILES:C[C@]12CC[C@@H]3[C@H]4CC[C@H](C[C@H]4CC[C@H]3[C@@H]1CC[C@]2(C#C)O)O
Uses A 3β-metabolite of progesterone receptor agonist Norethindrone (N676000) that acts as a estrogen receptor agonist in osteoblastic cells. It also has novel nongenomic endothelium-independent vasorelaxing effects.

Technology Process of Tetrahydronorethindrone

There total 6 articles about Tetrahydronorethindrone 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:

Reference yield: 59.0%