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Anadur

Base Information Edit
  • Chemical Name:Anadur
  • CAS No.:52279-57-9
  • Molecular Formula:C33H46 O4
  • Molecular Weight:506.726
  • Hs Code.:
  • European Community (EC) Number:257-810-4
  • UNII:602JJC2862
  • DSSTox Substance ID:DTXSID20966654
  • Nikkaji Number:J10.381K
  • Wikipedia:Nandrolone_hexyloxyphenylpropionate
  • Wikidata:Q27263147
  • NCI Thesaurus Code:C95971
  • Mol file:52279-57-9.mol
Anadur

Synonyms:19-nortestosterone 4-hexoxyphenylpropionate;Anadur;nandrolone p-hexyloxyphenylpropionate

Suppliers and Price of Anadur
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
  • American Custom Chemicals Corporation
  • NANDROLONE PARA-HEXYLOXYPHENYLPROPIONATE 95.00%
  • 5MG
  • $ 499.66
Total 5 raw suppliers
Chemical Property of Anadur Edit
Chemical Property:
  • Melting Point:53-55° 
  • Boiling Point:626.3°Cat760mmHg 
  • Flash Point:261.1°C 
  • PSA:52.60000 
  • Density:1.11g/cm3 
  • LogP:7.63190 
  • XLogP3:7.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:11
  • Exact Mass:506.33960994
  • Heavy Atom Count:37
  • Complexity:824
Purity/Quality:

99% *data from raw suppliers

NANDROLONE PARA-HEXYLOXYPHENYLPROPIONATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCOC1=CC=C(C=C1)CCC(=O)OC2CCC3C2(CCC4C3CCC5=CC(=O)CCC45)C
  • Isomeric SMILES:CCCCCCOC1=CC=C(C=C1)CCC(=O)O[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3CCC5=CC(=O)CC[C@H]45)C
Technology Process of Anadur

There total 2 articles about Anadur 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:
Aus 17β-Hydroxyestr-4-en-3-on, 3-(4-Hexyloxyphenyl)propionsaeure, /BRN= 610662/, p-Toluolsulfonsaeure (katalyt. Mengen), Py.;
Guidance literature:
19-Nortestosteron, <3-(4-Hexyloxy-phenyl>-propionsaeure-anhydrid, Pyridin;
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