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Tamoxifen acid

Base Information Edit
  • Chemical Name:Tamoxifen acid
  • CAS No.:97818-93-4
  • Molecular Formula:C24H22 O3
  • Molecular Weight:0
  • Hs Code.:2918990090
  • UNII:JMR6KG6KRJ
  • Nikkaji Number:J354.278E
  • ChEMBL ID:CHEMBL144704
  • Mol file:97818-93-4.mol
Tamoxifen acid

Synonyms:4-(1,2-diphenyl-1-butenyl)phenoxyacetic acid;tamoxifen acid

Suppliers and Price of Tamoxifen acid
Supply Marketing:Edit
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
  • Z-[4-(1,2-Diphenyl-1-butenyl)phenoxy]aceticAcid
  • 50mg
  • $ 245.00
Total 0 raw suppliers
Chemical Property of Tamoxifen acid Edit
Chemical Property:
  • Vapor Pressure:4E-11mmHg at 25°C 
  • Boiling Point:507.5°C at 760 mmHg 
  • Flash Point:172.9°C 
  • PSA:46.53000 
  • Density:1.154g/cm3 
  • LogP:5.51910 
  • XLogP3:6.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:358.15689456
  • Heavy Atom Count:27
  • Complexity:490
Purity/Quality:

Z-[4-(1,2-Diphenyl-1-butenyl)phenoxy]aceticAcid *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC(=C(C1=CC=CC=C1)C2=CC=C(C=C2)OCC(=O)O)C3=CC=CC=C3
  • Isomeric SMILES:CC/C(=C(\C1=CC=CC=C1)/C2=CC=C(C=C2)OCC(=O)O)/C3=CC=CC=C3
  • Uses Z-[4-(1,2-Diphenyl-1-butenyl)phenoxy]acetic Acid is an acidic metabolite of estrogenic Tamoxifen (T006000)
Technology Process of Tamoxifen acid

There total 12 articles about Tamoxifen acid 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 sodium hydroxide; In methanol; water; for 0.0833333h; Heating;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) Mg, BrCH2CH2Br, I2 / 1.) Et2O, reflux, 1 h, 2.) 16 h
2: conc. HCl / ethanol / 2 h / Heating
3: 1.) CH3ONa, 2.) 1.2M NaOH, Bu4NHSO4 / 1.) DMF, 35 deg C, 1 h, 2.) CH2Cl2, H2O, 10 min
4: 89 percent / NaOH / H2O; methanol / 0.08 h / Heating
With hydrogenchloride; sodium hydroxide; iodine; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; magnesium; ethylene dibromide; In methanol; ethanol; water;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) Mg, BrCH2CH2Br, I2 / 1.) Et2O, reflux, 1 h, 2.) 16 h
2: conc. HCl / ethanol / 2 h / Heating
3: 1.) CH3ONa, 2.) 1.2M NaOH, Bu4NHSO4 / 1.) DMF, 35 deg C, 1 h, 2.) CH2Cl2, H2O, 10 min
4: 89 percent / NaOH / H2O; methanol / 0.08 h / Heating
With hydrogenchloride; sodium hydroxide; iodine; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; magnesium; ethylene dibromide; In methanol; ethanol; water;
Refernces Edit
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