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trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane

Base Information Edit
  • Chemical Name:trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane
  • CAS No.:119880-44-3
  • Molecular Formula:C16H24OSi
  • Molecular Weight:260.451
  • Hs Code.:
  • Mol file:119880-44-3.mol
trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane Edit
Chemical Property:
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Technology Process of trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane

There total 6 articles about trans-1-benzoyl-1-(trimethylsilyl)-2-methylcyclopentane 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 pyridine; chromium(VI) oxide; In dichloromethane; for 0.666667h; Yield given;
DOI:10.1021/jo00267a032
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) LDA / 1.) -78 deg C, 20 min, 2.) from -30 to -10 deg C, 6 h
2: 82 percent / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C
3: 720 mg / CrO3, pyridine / CH2Cl2 / 1.5 h / 0 °C
4: 1.60 g / diethyl ether / 0.33 h / -78 °C
5: CrO3, pyridine / CH2Cl2 / 0.67 h
With pyridine; chromium(VI) oxide; diisobutylaluminium hydride; lithium diisopropyl amide; In diethyl ether; hexane; dichloromethane;
DOI:10.1021/jo00267a032
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) LDA / 1.) -78 deg C, 20 min, 2.) from -30 to -10 deg C, 6 h
2: 82 percent / Dibal-H / CH2Cl2; hexane / 4 h / -10 - 0 °C
3: 720 mg / CrO3, pyridine / CH2Cl2 / 1.5 h / 0 °C
4: 1.60 g / diethyl ether / 0.33 h / -78 °C
5: CrO3, pyridine / CH2Cl2 / 0.67 h
With pyridine; chromium(VI) oxide; diisobutylaluminium hydride; lithium diisopropyl amide; In diethyl ether; hexane; dichloromethane;
DOI:10.1021/jo00267a032
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