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C45H52N2O7Si

Base Information
  • Chemical Name:C45H52N2O7Si
  • CAS No.:886438-09-1
  • Molecular Formula:C45H52N2O7Si
  • Molecular Weight:761.003
  • Hs Code.:
C<sub>45</sub>H<sub>52</sub>N<sub>2</sub>O<sub>7</sub>Si

Synonyms:C45H52N2O7Si

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Chemical Property of C45H52N2O7Si
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Technology Process of C45H52N2O7Si

There total 14 articles about C45H52N2O7Si 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 triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
Guidance literature:
Multi-step reaction with 15 steps
1.1: m-chloroperbenzoic acid / 3 h / 25 - 64 °C
1.2: 78 percent / HCl / 12 h / 0 - 25 °C
2.1: 89 percent / triethylamine; 4-(dimethylamino)pyridine / 12 h / 25 °C
3.1: nBuLi / toluene; tetrahydrofuran / 0.33 h / -78 °C
3.2: 80 percent / toluene; tetrahydrofuran / 50 h / -78 °C
4.1: HCO2H; triethylamine / Noyori (R,R)-catalyst / dimethylformamide / 24 h / 0 - 40 °C
4.2: diphenylphosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene; dimethylformamide / 24 h / 50 °C
4.3: H2 / Pd/C / ethyl acetate / 15 h / 25 °C
5.1: acetic acid; NaCNBH3; MgSO4 / methanol / 4 h / 0 - 65 °C
6.1: tetrabutylammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
7.1: 84 percent / NaH / dimethylformamide / 2 h / 0 - 25 °C
8.1: 90 percent / HCl / dioxane / 72 h / 0 - 25 °C
9.1: 85 percent / bis(2-oxo-3-oxazolidinyl)phosphinic chloride; triethylamine / CH2Cl2 / 24 h / 0 - 25 °C
10.1: 90 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone; buffer solution / CH2Cl2 / 0.5 h / 25 °C / pH 7
11.1: 61 percent / Cu(OTf)2 / benzene / 0.25 h / 85 °C
12.1: 94 percent / Dess-Martin periodinane / CH2Cl2 / 5 h / 25 °C
13.1: 93 percent / tributyltin hydride; acetic acid / [(PPh3)2PdCl2] / 1 h / 0 - 25 °C
14.1: CHF2COOH; MgSO4 / benzene / 0.75 h / 100 °C
15.1: 100 percent / triethylamine / CH2Cl2 / 0.5 h / 0 °C
With hydrogenchloride; Difluoroacetic acid; dmap; n-butyllithium; formic acid; buffer solution; tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; copper(II) bis(trifluoromethanesulfonate); sodium hydride; sodium cyanoborohydride; magnesium sulfate; Dess-Martin periodane; acetic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; bis-triphenylphosphine-palladium(II) chloride; ((1R,2R)-N-p-toluenesulfonyl-1,2-diphenylethylenediamine)ruthenium chloride(I) (4-cymene); In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1002/anie.200503983
Guidance literature:
Multi-step reaction with 9 steps
1: 84 percent / NaH / dimethylformamide / 2 h / 0 - 25 °C
2: 90 percent / HCl / dioxane / 72 h / 0 - 25 °C
3: 85 percent / bis(2-oxo-3-oxazolidinyl)phosphinic chloride; triethylamine / CH2Cl2 / 24 h / 0 - 25 °C
4: 90 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone; buffer solution / CH2Cl2 / 0.5 h / 25 °C / pH 7
5: 61 percent / Cu(OTf)2 / benzene / 0.25 h / 85 °C
6: 94 percent / Dess-Martin periodinane / CH2Cl2 / 5 h / 25 °C
7: 93 percent / tributyltin hydride; acetic acid / [(PPh3)2PdCl2] / 1 h / 0 - 25 °C
8: CHF2COOH; MgSO4 / benzene / 0.75 h / 100 °C
9: 100 percent / triethylamine / CH2Cl2 / 0.5 h / 0 °C
With hydrogenchloride; Difluoroacetic acid; buffer solution; tri-n-butyl-tin hydride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; copper(II) bis(trifluoromethanesulfonate); sodium hydride; magnesium sulfate; Dess-Martin periodane; acetic acid; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1002/anie.200503983
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