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C48H54O8

Base Information Edit
  • Chemical Name:C48H54O8
  • CAS No.:189334-16-5
  • Molecular Formula:C48H54O8
  • Molecular Weight:758.952
  • Hs Code.:
  • Mol file:189334-16-5.mol
C<sub>48</sub>H<sub>54</sub>O<sub>8</sub>

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C48H54O8 Edit
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Technology Process of C48H54O8

There total 5 articles about C48H54O8 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 tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; 1.) 0 deg C, 1 h, 2.) r.t., 36 h;
DOI:10.1039/a700422b
Guidance literature:
Multi-step reaction with 5 steps
1: 72 percent / pyridine / 16 h / Heating
2: 76 percent / p-TsOH, ethylene glycol / CHCl3 / 1.5 h / 50 °C
3: 35 percent / PPh3*HBr / CHCl3 / 96 h / Ambient temperature
4: Bu4NF / tetrahydrofuran / 10 h / 60 °C
5: 61 percent / NaH, Bu4NI / dimethylformamide / 1.) 0 deg C, 1 h, 2.) r.t., 36 h
With pyridine; tetrabutyl ammonium fluoride; triphenylphosphine hydrobromide; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; ethylene glycol; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1039/a700422b
Guidance literature:
Multi-step reaction with 3 steps
1: 35 percent / PPh3*HBr / CHCl3 / 96 h / Ambient temperature
2: Bu4NF / tetrahydrofuran / 10 h / 60 °C
3: 61 percent / NaH, Bu4NI / dimethylformamide / 1.) 0 deg C, 1 h, 2.) r.t., 36 h
With tetrabutyl ammonium fluoride; triphenylphosphine hydrobromide; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1039/a700422b
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