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7-hydroxy-8-C-prenylisoflavanone

Base Information Edit
  • Chemical Name:7-hydroxy-8-C-prenylisoflavanone
  • CAS No.:105705-46-2
  • Molecular Formula:C20H20O3
  • Molecular Weight:308.377
  • Hs Code.:
  • Mol file:105705-46-2.mol
7-hydroxy-8-C-prenylisoflavanone

Synonyms:7-hydroxy-8-C-prenylisoflavanone

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Chemical Property of 7-hydroxy-8-C-prenylisoflavanone Edit
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Technology Process of 7-hydroxy-8-C-prenylisoflavanone

There total 3 articles about 7-hydroxy-8-C-prenylisoflavanone 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 tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III); In toluene; at 100 ℃; for 2h; Microwave irradiation;
DOI:10.1021/acs.orglett.7b01218
Guidance literature:
Multi-step reaction with 2 steps
1: tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 24 h / 0 °C
2: tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III) / toluene / 2 h / 100 °C / Microwave irradiation
With tetrakis(triphenylphosphine) palladium(0); tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III); In tetrahydrofuran; toluene;
DOI:10.1021/acs.orglett.7b01218
Guidance literature:
Multi-step reaction with 3 steps
1: hydrogenchloride / methanol; water / 72 h
2: tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 24 h / 0 °C
3: tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III) / toluene / 2 h / 100 °C / Microwave irradiation
With hydrogenchloride; tetrakis(triphenylphosphine) palladium(0); tris(6,6,7,7,8,8-heptafluoro-2,2-dimethyl-3,5-octadionato)europium(III); In tetrahydrofuran; methanol; water; toluene;
DOI:10.1021/acs.orglett.7b01218
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