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Stanolone benzoate

Base Information Edit
  • Chemical Name:Stanolone benzoate
  • CAS No.:1057-07-4
  • Molecular Formula:C26H34O3
  • Molecular Weight:394.554
  • Hs Code.:
  • European Community (EC) Number:213-891-8
  • NSC Number:69549
  • UNII:T74307G2D9
  • DSSTox Substance ID:DTXSID0036502
  • Nikkaji Number:J61.642G
  • Wikipedia:Androstanolone_benzoate
  • Wikidata:Q27116348
  • Mol file:1057-07-4.mol
Stanolone benzoate

Synonyms:dihydrotestosterone benzoate;stanolone benzoate

Suppliers and Price of Stanolone benzoate
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
  • DIHYDROTESTOSTERONE BENZOATE 98.00%
  • 5MG
  • $ 499.33
Total 22 raw suppliers
Chemical Property of Stanolone benzoate Edit
Chemical Property:
  • Vapor Pressure:2.4E-10mmHg at 25°C 
  • Melting Point:155 °C 
  • Refractive Index:1.569 
  • Boiling Point:505.6 °C at 760 mmHg 
  • Flash Point:216.7 °C 
  • PSA:43.37000 
  • Density:1.14 g/cm3 
  • LogP:5.82380 
  • XLogP3:5.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:394.25079494
  • Heavy Atom Count:29
  • Complexity:665
Purity/Quality:

98%,99%, *data from raw suppliers

DIHYDROTESTOSTERONE BENZOATE 98.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 63 
  • Safety Statements: 36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CCC(=O)CC1CCC3C2CCC4(C3CCC4OC(=O)C5=CC=CC=C5)C
  • Isomeric SMILES:C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4OC(=O)C5=CC=CC=C5)C
Technology Process of Stanolone benzoate

There total 13 articles about Stanolone benzoate 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:
In pyridine; at 60 ℃; for 2h;
DOI:10.1006/bioo.2001.1215
Guidance literature:
With 4-Benzoylpyridine; In acetone; at 20 ℃; for 46h; UV-irradiation; Inert atmosphere;
DOI:10.1021/acs.orglett.5b01550

Reference yield:

Guidance literature:
With chromic acid; acetic acid;
DOI:10.1002/hlca.19360190116
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