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(RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone

Base Information Edit
  • Chemical Name:(RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone
  • CAS No.:908368-68-3
  • Molecular Formula:C24H32O2
  • Molecular Weight:352.517
  • Hs Code.:
  • Mol file:908368-68-3.mol
(RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone

Synonyms:

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Chemical Property of (RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone Edit
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Technology Process of (RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone

There total 8 articles about (RS)-2-(3,7-dimethyloctyl)-4'-methoxybenzophenone 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:
Multi-step reaction with 3 steps
1.1: triphenylsilane; di-tert-butyl peroxide / 5 h / 140 °C
1.2: 36 percent / hydrochloric acid / diethyl ether / 70 h
2.1: oxalyl chloride / benzene / 1 h / Heating
3.1: 0.451 g / AlCl3 / 4 h / 140 °C
With aluminium trichloride; oxalyl dichloride; di-tert-butyl peroxide; HSiPh3; In benzene; 3.1: Friedel-Crafts reaction;
DOI:10.1021/jo060481q
Guidance literature:
Multi-step reaction with 2 steps
1: oxalyl chloride / benzene / 1 h / Heating
2: 0.451 g / AlCl3 / 4 h / 140 °C
With aluminium trichloride; oxalyl dichloride; In benzene; 2: Friedel-Crafts reaction;
DOI:10.1021/jo060481q
Guidance literature:
Multi-step reaction with 7 steps
1.1: H2
2.1: sodium iodide / acetone / 1 h / Heating
3.1: magnesium / diethyl ether / 20 °C
3.2: 50 percent / diethyl ether; tetrahydrofuran / 3 h / 20 °C
4.1: triphenylsilane; di-tert-butyl peroxide / 5 h / 140 °C
4.2: 36 percent / hydrochloric acid / diethyl ether / 70 h
5.1: oxalyl chloride / benzene / 1 h / Heating
6.1: 0.451 g / AlCl3 / 4 h / 140 °C
With aluminium trichloride; oxalyl dichloride; di-tert-butyl peroxide; hydrogen; magnesium; sodium iodide; HSiPh3; In diethyl ether; acetone; benzene; 2.1: Hunsdiecker reaction / 7.1: Friedel-Crafts reaction;
DOI:10.1021/jo060481q
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