3-O-Methyl 17|A-Estradiol

Base Information

Chemical Name:3-O-Methyl 17|A-Estradiol
CAS No.:3434-76-2
Molecular Formula:C24H34O3
Molecular Weight:286.414
Hs Code.:
DSSTox Substance ID:DTXSID90432639
Nikkaji Number:J617.982G
Wikidata:Q82246719
Mol file:3434-76-2.mol

Synonyms:3-O-Methyl 17|A-Estradiol;3434-76-2;3-O-Methyl 17alpha-estradiol;(8R,9S,13S,14S,17R)-3-methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-ol;SCHEMBL4750578;DTXSID90432639;ULAADVBNYHGIBP-FQBWVUSXSA-N;3-Methoxyestra-1,3,5(10)-trien-17alpha-ol;1,3,5(10)-Oestratrien-17.alpha.-ol, 3-methoxy;Estra-1,3,5(10)-trien-17.alpha.-ol, 3-methoxy-;Estra-1,3,5(10)-trien-17-ol, 3-methoxy-, (17.alpha.)-

Suppliers and Price of 3-O-Methyl 17|A-Estradiol

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

TRC
3-O-Methyl17α-Estradiol
2mg
$ 70.00

TRC
3-O-Methyl17α-Estradiol
50mg
$ 1320.00

American Custom Chemicals Corporation
3-O-METHYL-17-ALPHA-ESTRADIOL 95.00%
5MG
$ 502.87

Total 4 raw suppliers

Chemical Property of 3-O-Methyl 17|A-Estradiol

Chemical Property:

PSA：29.46000
LogP:3.91220
Solubility.:Chloroform, Tetrahydrofuran
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:286.193280068
Heavy Atom Count:21
Complexity:395

Purity/Quality:

97% ^*data from raw suppliers

3-O-Methyl17α-Estradiol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC
Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@H]2O)CCC4=C3C=CC(=C4)OC
Uses Estradiol derivative which shows antioxidant activity. Protected 3-Methoxyestradiol-d5.

Technology Process of 3-O-Methyl 17|A-Estradiol

There total 33 articles about 3-O-Methyl 17|A-Estradiol 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: 95.0%