Epimestrol

Base Information

Chemical Name:Epimestrol
CAS No.:7004-98-0
Molecular Formula:C19H26O3
Molecular Weight:302.414
Hs Code.:
European Community (EC) Number:230-278-0
NSC Number:55975
UNII:7IVE3SDZ38
DSSTox Substance ID:DTXSID90859807
Nikkaji Number:J8.873K
Wikipedia:Epimestrol
Wikidata:Q5383041
NCI Thesaurus Code:C80783
Metabolomics Workbench ID:154198
ChEMBL ID:CHEMBL2106236
Mol file:7004-98-0.mol

Synonyms:Epimestrol;Stimuvol

Suppliers and Price of Epimestrol

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

American Custom Chemicals Corporation
EPIMESTROL 95.00%
5MG
$ 495.44

Total 11 raw suppliers

Chemical Property of Epimestrol

Chemical Property:

Vapor Pressure:6.48E-09mmHg at 25°C
Refractive Index:1.588
Boiling Point:450.8 °C at 760 mmHg
Flash Point:226.4 °C
PSA：49.69000
Density:1.185 g/cm³
LogP:2.88300
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:302.18819469
Heavy Atom Count:22
Complexity:425

Purity/Quality:

99% ^*data from raw suppliers

EPIMESTROL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC3C(C1CC(C2O)O)CCC4=C3C=CC(=C4)OC
Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@H]2O)O)CCC4=C3C=CC(=C4)OC
Uses Anterior pituitary activator.
Therapeutic Function Anterior pituitary activator

Technology Process of Epimestrol

There total 8 articles about Epimestrol 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: 89.0%

: 81163-66-8
3-Methoxy-oestra-1,3,5(10)-trieno-<16α,17α-d>-dioxol-2'-on

: 7004-98-0
3-methoxy-1,3,5(10)-estratriene-16α,17α-diol

Guidance literature:: With potassium carbonate; In ethanol; water; for 5h; Heating;

Reference yield:

: 28336-32-5
16α,17α-Epoxy-3-methoxyestra-1,3,5(10)-triene

: 7004-98-0
3-methoxy-1,3,5(10)-estratriene-16α,17α-diol

Guidance literature:: Multi-step reaction with 4 steps

1: HBr

2: 55 percent / triethylamine / benzene / 9 h / Heating

3: 70 percent / 80percent aq. EtOH / 6 h / Heating

4: 89 percent / K₂CO₃ / ethanol; H₂O / 5 h / Heating

With ethanol; hydrogen bromide; potassium carbonate; triethylamine; In ethanol; water; benzene;

Reference yield:

: 55821-45-9
16β-Brom-3-methoxy-oestra-1,3,5(10)-trien-17α-ol

: 7004-98-0
3-methoxy-1,3,5(10)-estratriene-16α,17α-diol

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / triethylamine / benzene / 9 h / Heating

2: 70 percent / 80percent aq. EtOH / 6 h / Heating

3: 89 percent / K₂CO₃ / ethanol; H₂O / 5 h / Heating

With ethanol; potassium carbonate; triethylamine; In ethanol; water; benzene;