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(1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene

Base Information
  • Chemical Name:(1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene
  • CAS No.:66606-89-1
  • Molecular Formula:C26H28O2
  • Molecular Weight:372.507
  • Hs Code.:
(1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.0<sup>2,5</sup>]deca-3,7-diene

Synonyms:(1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene

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Chemical Property of (1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene
Chemical Property:
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Technology Process of (1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene

There total 6 articles about (1S,2S,5R,6R)-3,8-Bis-(4-methoxy-phenyl)-4,7-dimethyl-tricyclo[4.2.2.02,5]deca-3,7-diene 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 p-benzoquinone; In acetonitrile; at 23 ℃; for 0.25h; Product distribution; Mechanism; Quantum yield; Irradiation; reaction quenchers (piperilene, Et3N); other weak electron acceptor (9,10-anthraquinone); other reaction types under other conditions (without irradiation, in presence of various quinones or tetracyanoethylene); a series of phenylated cage compounds;
DOI:10.1021/ja00393a029
Guidance literature:
With tetraethylammonium perchlorate; In acetonitrile; for 0.166667h; anodic oxidation with Pt gauze electrode;
DOI:10.1246/cl.1984.1553
Guidance literature:
With phenanthrene-9,10-dicarbonitrile; In benzene; Irradiation;
DOI:10.1021/ja00334a070
upstream raw materials:

C26H28O2

C32H28N4O2

C26H28O2

C26H28O2

Downstream raw materials:

C32H28N4O2

C26H28O2

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