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(1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide

Base Information Edit
  • Chemical Name:(1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide
  • CAS No.:220571-38-0
  • Molecular Formula:C38H46O3Si2
  • Molecular Weight:606.952
  • Hs Code.:
  • Mol file:220571-38-0.mol
(1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide

Synonyms:(1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide

Suppliers and Price of (1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide Edit
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Technology Process of (1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide

There total 3 articles about (1SR,2RS,4RS,5SR)-4,5-bis(tert-butyldiphenylsilyloxy)cyclohexene oxide 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 sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 20h; Ambient temperature;
DOI:10.1016/S0040-4039(98)02319-3
Guidance literature:
Multi-step reaction with 3 steps
1.1: KIO3; I2; AcOH / 4 h / 60 °C
1.2: potassium acetate / acetic acid / 4 h / Heating
1.3: 74 percent / Amberlite IRA(OH); methanol / tetrahydrofuran / 16 h / 20 °C
2.1: 94 percent / imidazole / CH2Cl2 / 20 h / 20 °C
3.1: 92 percent / m-CPBA; NaHCO3 / CH2Cl2 / 20 h / 20 °C
With 1H-imidazole; potassium iodate; iodine; sodium hydrogencarbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1016/S0040-4020(02)00370-8
Guidance literature:
Multi-step reaction with 2 steps
1: 94 percent / imidazole / CH2Cl2 / 20 h / 20 °C
2: 92 percent / m-CPBA; NaHCO3 / CH2Cl2 / 20 h / 20 °C
With 1H-imidazole; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1016/S0040-4020(02)00370-8
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