3-O-Benzyl Estradiol

Base Information

Chemical Name:3-O-Benzyl Estradiol
CAS No.:14982-15-1
Molecular Formula:C25H30O2
Molecular Weight:362.512
Hs Code.:
DSSTox Substance ID:DTXSID00461450
Nikkaji Number:J730.998H
Wikidata:Q82285799
Mol file:14982-15-1.mol

Synonyms:3-O-Benzyl Estradiol;14982-15-1;(8R,9S,13S,14S,17S)-13-methyl-3-phenylmethoxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-ol;SCHEMBL3350939;DTXSID00461450;3-benzyloxyestra-1,3,5(10)-trien-17beta-ol;3-Benzyloxy-17beta-hydroxyestra-1,3,5(10)-triene;3-(Phenylmethoxy)estra-1,3,5(10)-trien-17.beta.-ol

Suppliers and Price of 3-O-Benzyl 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-BenzylEstradiol
250 mg
$ 1230.00

TRC
3-O-BenzylEstradiol
25 mg
$ 155.00

Biosynth Carbosynth
3-O-Benzyl estradiol
50 mg
$ 462.00

Biosynth Carbosynth
3-O-Benzyl estradiol
25 mg
$ 254.50

Biosynth Carbosynth
3-O-Benzyl estradiol
10 mg
$ 139.80

Biosynth Carbosynth
3-O-Benzyl estradiol
250 mg
$ 1530.00

Biosynth Carbosynth
3-O-Benzyl estradiol
100 mg
$ 840.00

AK Scientific
3-O-BenzylEstradiol
50mg
$ 673.00

Total 10 raw suppliers

Chemical Property of 3-O-Benzyl Estradiol

Chemical Property:

PSA：29.46000
LogP:5.48260
Solubility.:Dichloromethane, Methanol
XLogP3:4.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:362.224580195
Heavy Atom Count:27
Complexity:513

Purity/Quality:

99% ^*data from raw suppliers

3-O-BenzylEstradiol ^*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)OCC5=CC=CC=C5
Isomeric SMILES:C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C3C=CC(=C4)OCC5=CC=CC=C5

Technology Process of 3-O-Benzyl Estradiol

There total 22 articles about 3-O-Benzyl 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: 100.0%

: 858-98-0
3-benzyloxyestra-1,3,5⁽¹⁰⁾-trien-17-one

: 14982-15-1
3-benzyloxyestra-1,3,5(10)-trien-17β-ol

Guidance literature:: With sodium borohydrid; In tetrahydrofuran; methanol;

Reference yield: 97.0%

: 50-28-2
estradiol

: 100-39-0
benzyl bromide

: 14982-15-1
3-benzyloxyestra-1,3,5(10)-trien-17β-ol

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In acetone; Reflux;

Reference yield: 94.0%

: 50-28-2
estradiol

: 100-44-7
benzyl chloride

: 14982-15-1
3-benzyloxyestra-1,3,5(10)-trien-17β-ol

Guidance literature:: With tetra-(n-butyl)ammonium iodide; potassium hydroxide; In ethanol; water; for 12h; Reflux; Inert atmosphere;
DOI:10.1016/j.steroids.2009.09.013