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10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane

Base Information Edit
  • Chemical Name:10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane
  • CAS No.:497967-74-5
  • Molecular Formula:C16H29NO5
  • Molecular Weight:315.41
  • Hs Code.:
  • Mol file:497967-74-5.mol
10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane

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Suppliers and Price of 10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane Edit
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Technology Process of 10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane

There total 1 articles about 10,13,16,19,22-Pentaoxa-7-azadispiro[5.1.12.2]docosane 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:
Multi-step reaction with 6 steps
1: hydrochloric acid / H2O / 5 h / 55 °C
2: 3.32 g / NaHCO3 / H2O; dioxane / 4 h / 0 - 20 °C
3: 72 percent / TEMPO; NaHCO3; NaClO / H2O; acetonitrile / 20 °C
4: 99 percent / diethyl ether; CH2Cl2 / 0.25 h
5: 99 percent / H2 / 10 percent Pd/C / methanol
6: 73 percent / benzotriazol-1-yl-oxy-tripyrrolidinophosphonium PF6(1-); diisopropylethylamine / CH2Cl2 / 120 h / 20 °C
With hydrogenchloride; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; hydrogen; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In 1,4-dioxane; methanol; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4020(02)01065-7
Guidance literature:
Multi-step reaction with 4 steps
1: hydrochloric acid / H2O / 5 h / 55 °C
2: 3.32 g / NaHCO3 / H2O; dioxane / 4 h / 0 - 20 °C
3: 72 percent / TEMPO; NaHCO3; NaClO / H2O; acetonitrile / 20 °C
4: 99 percent / diethyl ether; CH2Cl2 / 0.25 h
With hydrogenchloride; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; sodium hydrogencarbonate; In 1,4-dioxane; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4020(02)01065-7
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