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tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate

Base Information
  • Chemical Name:tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate
  • CAS No.:279671-11-3
  • Molecular Formula:C15H27NO4
  • Molecular Weight:285.384
  • Hs Code.:
tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate

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Chemical Property of tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate
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Technology Process of tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate

There total 7 articles about tert-butyl cyclopropyl-[(2,2-dimethylpropionyl)-methyl-aminooxy]-acetate 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:
tert-butyl cyclopropyl-(2,2-dimethyl-propionylaminooxy)-acetate; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃;
methyl iodide; In N,N-dimethyl-formamide; at 20 ℃; for 2h; Further stages.;
DOI:10.1021/ol991392l
Guidance literature:
Multi-step reaction with 7 steps
1.1: KMnO4; Na2CO3 / H2O / 24 h / 20 °C
2.1: (COCl)2; DMF / CH2Cl2 / 2.5 h / 20 °C
2.2: 64 percent / pyridine / CH2Cl2 / 20 h / 20 °C
3.1: 75 percent / NaCNBH3; HCl / methanol / 0.25 h / 20 °C
4.1: 71 percent / PPh3; DEAD / tetrahydrofuran / 23 h / 20 °C
5.1: NH2NH2*H2O / methanol / 0.25 h / 20 °C
6.1: 325 mg / aq. NaHCO3 / CH2Cl2 / 3 h / 20 °C
7.1: NaH / dimethylformamide / 20 °C
7.2: 56 percent / dimethylformamide / 2 h / 20 °C
With hydrogenchloride; potassium permanganate; oxalyl dichloride; sodium hydride; sodium cyanoborohydride; sodium hydrogencarbonate; sodium carbonate; hydrazine hydrate; N,N-dimethyl-formamide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 1.1: Oxidation / 2.1: Substitution / 2.2: Esterification / 3.1: Reduction / 4.1: Condensation / 5.1: Substitution / 6.1: Condensation / 7.1: Metallation / 7.2: Methylation;
DOI:10.1021/ol991392l
Guidance literature:
Multi-step reaction with 6 steps
1.1: (COCl)2; DMF / CH2Cl2 / 2.5 h / 20 °C
1.2: 64 percent / pyridine / CH2Cl2 / 20 h / 20 °C
2.1: 75 percent / NaCNBH3; HCl / methanol / 0.25 h / 20 °C
3.1: 71 percent / PPh3; DEAD / tetrahydrofuran / 23 h / 20 °C
4.1: NH2NH2*H2O / methanol / 0.25 h / 20 °C
5.1: 325 mg / aq. NaHCO3 / CH2Cl2 / 3 h / 20 °C
6.1: NaH / dimethylformamide / 20 °C
6.2: 56 percent / dimethylformamide / 2 h / 20 °C
With hydrogenchloride; oxalyl dichloride; sodium hydride; sodium cyanoborohydride; sodium hydrogencarbonate; hydrazine hydrate; N,N-dimethyl-formamide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Substitution / 1.2: Esterification / 2.1: Reduction / 3.1: Condensation / 4.1: Substitution / 5.1: Condensation / 6.1: Metallation / 6.2: Methylation;
DOI:10.1021/ol991392l
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