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3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile

Base Information
  • Chemical Name:3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile
  • CAS No.:925463-64-5
  • Molecular Formula:C37H48N2O6SSi
  • Molecular Weight:676.949
  • Hs Code.:
3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1<i>H</i>-indol-4-yl]-2-methoxymethoxy-propionitrile

Synonyms:3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile

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Chemical Property of 3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile
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Technology Process of 3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile

There total 14 articles about 3-[7-benzyloxy-3-methyl-1-(toluene-4-sulfonyl)-5-triisopropylsilanyloxy-1H-indol-4-yl]-2-methoxymethoxy-propionitrile 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 10 steps
1: 84 percent / pyridine / CH2Cl2 / 4 h / 20 °C
2: 96 percent / sodium periodate on silica gel / CH2Cl2 / 4 h
3: CH2Cl2 / 15 h / 20 °C
4: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.33 h / 0 °C
5: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C
6: osmium tetroxide; N-methylmorpholine N-oxide / tetrahydrofuran; H2O
7: sodium periodate on silica gel / CH2Cl2 / 2 h
8: 3.00 g / sulfuric acid / tetrahydrofuran / 5 h
9: triethylamine / CH2Cl2 / 2 h
10: 1.79 g / trifluoromethanesulfonic acid / 1 h
With pyridine; sodium periodate; osmium(VIII) oxide; trifluorormethanesulfonic acid; sulfuric acid; sodium hydride; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; dichloromethane; water; 3: Diels-Alder reaction;
DOI:10.1021/jo062064j
Guidance literature:
Multi-step reaction with 11 steps
1: sodium borohydride; nickel(II) chloride hexahydrate / tetrahydrofuran; methanol
2: 84 percent / pyridine / CH2Cl2 / 4 h / 20 °C
3: 96 percent / sodium periodate on silica gel / CH2Cl2 / 4 h
4: CH2Cl2 / 15 h / 20 °C
5: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.33 h / 0 °C
6: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C
7: osmium tetroxide; N-methylmorpholine N-oxide / tetrahydrofuran; H2O
8: sodium periodate on silica gel / CH2Cl2 / 2 h
9: 3.00 g / sulfuric acid / tetrahydrofuran / 5 h
10: triethylamine / CH2Cl2 / 2 h
11: 1.79 g / trifluoromethanesulfonic acid / 1 h
With pyridine; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; trifluorormethanesulfonic acid; sulfuric acid; sodium hydride; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; water; 4: Diels-Alder reaction;
DOI:10.1021/jo062064j
Guidance literature:
Multi-step reaction with 9 steps
1: 96 percent / sodium periodate on silica gel / CH2Cl2 / 4 h
2: CH2Cl2 / 15 h / 20 °C
3: 3.08 g / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH2Cl2 / 0.33 h / 0 °C
4: 94 percent / sodium hydride / tetrahydrofuran / 0 - 20 °C
5: osmium tetroxide; N-methylmorpholine N-oxide / tetrahydrofuran; H2O
6: sodium periodate on silica gel / CH2Cl2 / 2 h
7: 3.00 g / sulfuric acid / tetrahydrofuran / 5 h
8: triethylamine / CH2Cl2 / 2 h
9: 1.79 g / trifluoromethanesulfonic acid / 1 h
With sodium periodate; osmium(VIII) oxide; trifluorormethanesulfonic acid; sulfuric acid; sodium hydride; 4-methylmorpholine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; In tetrahydrofuran; dichloromethane; water; 2: Diels-Alder reaction;
DOI:10.1021/jo062064j
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