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methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate

Base Information Edit
  • Chemical Name:methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate
  • CAS No.:247035-22-9
  • Molecular Formula:C13H17FN2O2
  • Molecular Weight:252.289
  • Hs Code.:
  • Mol file:247035-22-9.mol
methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate

Synonyms:methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate Edit
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Technology Process of methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate

There total 6 articles about methyl (4-aminopiperidin-1-yl)-3-fluorobenzoate 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 hydrogen; acetic acid; palladium on activated charcoal; In 1,4-dioxane; at 20 ℃; for 4h;
DOI:10.1016/j.bmc.2005.10.061
Guidance literature:
Multi-step reaction with 4 steps
1: 87 percent / dimethylsulfoxide / 72 h / 120 °C
2: 92 percent / Et3N / CH2Cl2 / 1 h
3: NaN3 / dimethylformamide / 5 h / 80 °C
4: 85 percent / H2; AcOH / Pd/C / dioxane / 4 h / 20 °C
With sodium azide; hydrogen; acetic acid; triethylamine; palladium on activated charcoal; In 1,4-dioxane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.10.061
Guidance literature:
Multi-step reaction with 3 steps
1: 92 percent / Et3N / CH2Cl2 / 1 h
2: NaN3 / dimethylformamide / 5 h / 80 °C
3: 85 percent / H2; AcOH / Pd/C / dioxane / 4 h / 20 °C
With sodium azide; hydrogen; acetic acid; triethylamine; palladium on activated charcoal; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.10.061
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