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Dichamanetin

Base Information
  • Chemical Name:Dichamanetin
  • CAS No.:58779-09-2
  • Molecular Formula:C29H24O6
  • Molecular Weight:468.506
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90207506
  • Nikkaji Number:J61.219G
  • Wikidata:Q27138022
  • ChEMBL ID:CHEMBL1835968
  • Mol file:58779-09-2.mol
Dichamanetin

Synonyms:dichamanetin

Suppliers and Price of Dichamanetin
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
Total 1 raw suppliers
Chemical Property of Dichamanetin
Chemical Property:
  • Vapor Pressure:7.39E-24mmHg at 25°C 
  • Boiling Point:759.2°Cat760mmHg 
  • Flash Point:258.3°C 
  • PSA:107.22000 
  • Density:1.375g/cm3 
  • LogP:5.39710 
  • XLogP3:5.9
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:468.15728848
  • Heavy Atom Count:35
  • Complexity:707
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(OC2=C(C(=C(C(=C2C1=O)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O)C5=CC=CC=C5
  • Isomeric SMILES:C1[C@H](OC2=C(C(=C(C(=C2C1=O)O)CC3=CC=CC=C3O)O)CC4=CC=CC=C4O)C5=CC=CC=C5
Technology Process of Dichamanetin

There total 6 articles about Dichamanetin 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 zinc(II) chloride; In 1,4-dioxane; at 100 ℃; for 24h;
DOI:10.1021/ol052269z
Guidance literature:
Multi-step reaction with 2 steps
1: 90 percent / hydrochloric acid / methanol / 0.5 h / Heating
2: 59 percent / ZnCl2 / dioxane / 24 h / 100 °C
With hydrogenchloride; zinc(II) chloride; In 1,4-dioxane; methanol;
DOI:10.1021/ol052269z
Guidance literature:
Multi-step reaction with 5 steps
1: 73 percent / ethyldiisopropylamine / tetrahydrofuran / 12 h / 0 °C
2: 85 percent / KOH / ethanol; H2O / 48 h / 0 - 20 °C
3: 72 percent / sodium acetate / methanol / 48 h / Heating
4: 90 percent / hydrochloric acid / methanol / 0.5 h / Heating
5: 59 percent / ZnCl2 / dioxane / 24 h / 100 °C
With hydrogenchloride; potassium hydroxide; sodium acetate; N-ethyl-N,N-diisopropylamine; zinc(II) chloride; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; water;
DOI:10.1021/ol052269z
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