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Castelanone

Base Information Edit
  • Chemical Name:Castelanone
  • CAS No.:70424-54-3
  • Molecular Formula:C25H34O9
  • Molecular Weight:478.53206
  • Hs Code.:
  • NSC Number:312626
  • DSSTox Substance ID:DTXSID20990631
  • Nikkaji Number:J39.951E
  • Wikidata:Q27106091
  • Mol file:70424-54-3.mol
Castelanone

Synonyms:castelanone

Suppliers and Price of Castelanone
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
Total 0 raw suppliers
Chemical Property of Castelanone Edit
Chemical Property:
  • Vapor Pressure:5.94E-21mmHg at 25°C 
  • Boiling Point:672.3°C at 760 mmHg 
  • Flash Point:226.2°C 
  • PSA:139.59000 
  • Density:1.38g/cm3 
  • LogP:0.73400 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:4
  • Exact Mass:478.22028266
  • Heavy Atom Count:34
  • Complexity:973
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O)OC(=O)CC(C)C
  • Isomeric SMILES:C[C@@H]1[C@@H]2[C@H](C(=O)O[C@H]3[C@@]24CO[C@@]([C@@H]1O)([C@@H]4[C@@]5([C@@H](C3)C(=CC(=O)[C@H]5O)C)C)O)OC(=O)CC(C)C
Technology Process of Castelanone

There total 8 articles about Castelanone 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 tetrabutyl ammonium fluoride; In tetrahydrofuran; for 0.5h; Yield given; Ambient temperature;
DOI:10.1016/S0040-4039(00)87397-9
Guidance literature:
With hydrogen fluoride; In acetonitrile; for 6h; Yield given; Ambient temperature;
DOI:10.1016/S0040-4020(01)81638-0
Guidance literature:
Multi-step reaction with 7 steps
1: 88 percent / imidazole / dimethylformamide / 48 h / Ambient temperature
2: pyridine / CHCl3 / 2 h / Ambient temperature
3: 1.) lithium diisopropylamide; 2.) MoO5, pyridine, HMPA / 1.) THF, -78 deg C, 2 h; 2.) THF, -44 deg C, 4 h
4: pyridine; CH2Cl2 / 5 h / Ambient temperature
5: 1N HCl / methanol / 0.25 h / Ambient temperature
6: H2CrO4 / acetone / 0.05 h / Ambient temperature
7: tetrabutylammonium fluoride / tetrahydrofuran / 0.5 h / Ambient temperature
With pyridine; 1H-imidazole; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; tetrabutyl ammonium fluoride; chromic acid; {MoO(O2)2}; lithium diisopropyl amide; In tetrahydrofuran; pyridine; methanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0040-4039(00)87397-9
upstream raw materials:

C34H56O9Si2

chaparrin

C32H56O7Si2

C35H64O7Si3

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