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(1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.09,11>dodecane

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  • Chemical Name:(1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.09,11>dodecane
  • CAS No.:117641-41-5
  • Molecular Formula:C24H39N3O7Si2
  • Molecular Weight:537.761
  • Hs Code.:
  • Mol file:117641-41-5.mol
(1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.0<sup>9,11</sup>>dodecane

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Chemical Property of (1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.09,11>dodecane Edit
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Technology Process of (1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.09,11>dodecane

There total 12 articles about (1S,8S,9R,11S)-10-(2,4-dinitroanilino)-3,3,5,5-tetraisopropyl-2,4,6-trioxa-10-aza-3,5-disilatricyclo<6.4.0.09,11>dodecane 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 5 steps
1: 1.58 g / CH2Cl2; pyridine / 5 h
2: 1.29 g / sodium azide, ammonium chloride / H2O; ethanol / 4 h / Heating
3: 0.63 g / H2 / Lindlar catalyst / ethanol / 2 h / 760 Torr
4: 0.63 g / Na2CO3 / dimethylformamide / 18 h / Ambient temperature
5: 0.125 g / diethylaminosulphur trifluoride / CH2Cl2 / 0.17 h
With sodium azide; diethylamino-sulfur trifluoride; ammonium chloride; hydrogen; sodium carbonate; Lindlar's catalyst; In pyridine; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1039/P19880000549
Guidance literature:
Multi-step reaction with 9 steps
1: 15.8 g / (-)-diisopinan-3-ylborane / tetrahydrofuran / 1.) -60 deg C, 1 h; 2.) 5 deg C, 18 h
2: 12.0 g / t-butyl hydroperoxide, vanadium(V)acetylacetonate / 1,2-dichloro-ethane / 2.75 h / 30 °C
3: 1.) NaH; 2.) tetrabutylammonium iodide / 1.) THF, 2 h; 1.) THF, 2.5 h
4: 100 percent / H2 / 10percent Pd/C
5: 1.58 g / CH2Cl2; pyridine / 5 h
6: 1.29 g / sodium azide, ammonium chloride / H2O; ethanol / 4 h / Heating
7: 0.63 g / H2 / Lindlar catalyst / ethanol / 2 h / 760 Torr
8: 0.63 g / Na2CO3 / dimethylformamide / 18 h / Ambient temperature
9: 0.125 g / diethylaminosulphur trifluoride / CH2Cl2 / 0.17 h
With tert.-butylhydroperoxide; sodium azide; tris(acetylacetonato)vanadium(III); diethylamino-sulfur trifluoride; (-)-diisopinan-3-ylborane; ammonium chloride; hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium carbonate; palladium on activated charcoal; Lindlar's catalyst; In tetrahydrofuran; pyridine; ethanol; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1039/P19880000549
Guidance literature:
Multi-step reaction with 6 steps
1: 100 percent / H2 / 10percent Pd/C
2: 1.58 g / CH2Cl2; pyridine / 5 h
3: 1.29 g / sodium azide, ammonium chloride / H2O; ethanol / 4 h / Heating
4: 0.63 g / H2 / Lindlar catalyst / ethanol / 2 h / 760 Torr
5: 0.63 g / Na2CO3 / dimethylformamide / 18 h / Ambient temperature
6: 0.125 g / diethylaminosulphur trifluoride / CH2Cl2 / 0.17 h
With sodium azide; diethylamino-sulfur trifluoride; ammonium chloride; hydrogen; sodium carbonate; palladium on activated charcoal; Lindlar's catalyst; In pyridine; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1039/P19880000549
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