Trioxifene

Base Information

Chemical Name:Trioxifene
CAS No.:63619-84-1
Molecular Formula:C31H35NO6S
Molecular Weight:453.581
Hs Code.:
UNII:R0130F043H
DSSTox Substance ID:DTXSID30212997
Nikkaji Number:J19.668A
Wikipedia:Trioxifene
Wikidata:Q7843173
NCI Thesaurus Code:C1266
ChEMBL ID:CHEMBL110057

Synonyms:3,4-dihydro-2-(p-methoxyphenyl)-1-naphthyl p-(2-(1-pyrrolidinyl)ethoxy)phenylketone;Lilly 133314;Lilly 88571;LY 133314;LY 88571;trioxifene;trioxifene mesylate;trioxifene methanesulfonate

Suppliers and Price of Trioxifene

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
Trioxifene
50mg
$ 1320.00

Medical Isotopes, Inc.
Trioxifene
50 mg
$ 2200.00

American Custom Chemicals Corporation
TRIOXIFENE 95.00%
5MG
$ 496.74

Total 10 raw suppliers

Chemical Property of Trioxifene

Chemical Property:

Vapor Pressure:5.91E-16mmHg at 25°C
Boiling Point:633.5°Cat760mmHg
Flash Point:336.9°C
PSA：38.77000
Density:g/cm³
LogP:5.84760
XLogP3:5.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:453.23039385
Heavy Atom Count:34
Complexity:696

Purity/Quality:

99% ,98%,Electron Grade , ^*data from raw suppliers

Trioxifene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2=C(C3=CC=CC=C3CC2)C(=O)C4=CC=C(C=C4)OCCN5CCCC5
Uses Trioxifene (LY-133,314) is a selective estrogen receptor modulator (SERM) with competitive binding activity against estradiol for estrogen receptor {α} (ER{α}) and antagonistic activity against ER{α}-mediated gene expression. It may be useful for the treatment of breast cancer.

Technology Process of Trioxifene

There total 1 articles about Trioxifene 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: