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<2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate

Base Information
  • Chemical Name:<2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate
  • CAS No.:131729-77-6
  • Molecular Formula:C28H45NO7
  • Molecular Weight:507.668
  • Hs Code.:
<2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate

Synonyms:<2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of <2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate
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Technology Process of <2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate

There total 4 articles about <2-<<(N-pentadecylcarbamoyl)oxy>methyl>-1,3-dioxolan-4-yl>methyl phenylcarbonate 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; hydrogenchloride; In chloroform;
Guidance literature:
Multi-step reaction with 3 steps
1: camphorsulfonic acid (CSA) / toluene / 18 h / Ambient temperature
2: 93 percent / H2 / 5percent Pd/C / CH2Cl2; ethanol / 18 h / 4137.2 Torr
3: pyridine / CHCl3 / 6 h / Heating
With pyridine; camphor-10-sulfonic acid; hydrogen; palladium on activated charcoal; In ethanol; dichloromethane; chloroform; toluene;
DOI:10.1021/jm00105a058
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / H2 / 5percent Pd/C / CH2Cl2; ethanol / 18 h / 4137.2 Torr
2: pyridine / CHCl3 / 6 h / Heating
With pyridine; hydrogen; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jm00105a058
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