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Zindoxifene

Base Information
  • Chemical Name:Zindoxifene
  • CAS No.:86111-26-4
  • Molecular Formula:C21H21NO4
  • Molecular Weight:351.402
  • Hs Code.:2933990090
  • NSC Number:341952
  • UNII:1IRS95M8DN
  • DSSTox Substance ID:DTXSID60235396
  • Nikkaji Number:J436.824J
  • Wikipedia:Zindoxifene
  • Wikidata:Q27116390
  • NCI Thesaurus Code:C66696
  • ChEMBL ID:CHEMBL32227
  • Mol file:86111-26-4.mol
Zindoxifene

Synonyms:5-acetoxy-2-(4-acetoxyphenyl)-1-ethyl-3-methylindole;D 16726;D-16762;zindoxifene

Suppliers and Price of Zindoxifene
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
  • ZINDOXIFENE 95.00%
  • 5MG
  • $ 501.66
Total 20 raw suppliers
Chemical Property of Zindoxifene
Chemical Property:
  • Vapor Pressure:1.88E-10mmHg at 25°C 
  • Boiling Point:508.3°Cat760mmHg 
  • Flash Point:261.2°C 
  • PSA:57.53000 
  • Density:1.17g/cm3 
  • LogP:4.48720 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:351.14705815
  • Heavy Atom Count:26
  • Complexity:514
Purity/Quality:

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

ZINDOXIFENE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN1C2=C(C=C(C=C2)OC(=O)C)C(=C1C3=CC=C(C=C3)OC(=O)C)C
Technology Process of Zindoxifene

There total 14 articles about Zindoxifene 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:
Guidance literature:
With 4-(1,1-dimethylethyl)benzoic acid; In dichloromethane; at 40 ℃; for 24h; Inert atmosphere; Glovebox; Schlenk technique;
DOI:10.1039/c9cc04529e
Guidance literature:
Multi-step reaction with 2 steps
1: BBr3 / CH2Cl2 / -60 - 20 °C
2: pyridine / 2 h / Heating
With pyridine; boron tribromide; In dichloromethane;
DOI:10.1021/jm00377a011
Guidance literature:
Multi-step reaction with 4 steps
1: N,N-dimethylaniline / 170 °C
2: 1.) Na/liquid NH3 / 1.) THF, -70 deg C, 30 min, 2.) THF, -70 deg C, 30 min
3: BBr3 / CH2Cl2 / -60 - 20 °C
4: pyridine / 2 h / Heating
With pyridine; ammonia; sodium; boron tribromide; N,N-dimethyl-aniline; In dichloromethane;
DOI:10.1021/jm00377a011
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