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Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid

Base Information
  • Chemical Name:Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid
  • CAS No.:115096-37-2
  • Molecular Formula:C24H30O4
  • Molecular Weight:382.5
  • Hs Code.:
Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid

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Chemical Property of Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid
Chemical Property:
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Technology Process of Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid

There total 10 articles about Ethyl-3,6-di-O-benzyl-2,4-didesoxy-2-methyl-4-methylen-β-DL-lyxo-hexopyranosid 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 7 steps
1: 99 percent / hydroquinone / 96 h / 6000480 Torr / Ambient temperature
2: 91 percent / K2CO3 / methanol / 20 h / Ambient temperature
3: 1.) NaH / 1.) DMF, 0 deg C, 1 h; 2.) 15 h
4: 98 percent / Raney-Nickel / tetrahydrofuran / 8 h / Ambient temperature
5: 1.) BH3*S(CH3)2; 2.) 30percent H2O2/10percent NaOH / 1.) THF, 15 h, -10 deg C; 2.) 0 deg C to room temp., 3 h
6: 74 percent / pyridinium chloro-chromate / CH2Cl2 / 144 h / Ambient temperature
7: 1.) 1.6M n-C4H9Li/n-hexane / 1.) THF, 45 min; 2.) THF, 19 h, room temp.
With sodium hydroxide; n-butyllithium; hexane; dimethylsulfide borane complex; dihydrogen peroxide; nickel; sodium hydride; potassium carbonate; pyridinium chlorochromate; hydroquinone; In tetrahydrofuran; methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 7 steps
1: 99 percent / hydroquinone / 96 h / 6000480 Torr / Ambient temperature
2: 91 percent / K2CO3 / methanol / 20 h / Ambient temperature
3: 1.) NaH / 1.) DMF, 0 deg C, 1 h; 2.) 15 h
4: 98 percent / Raney-Nickel / tetrahydrofuran / 8 h / Ambient temperature
5: 1.) BH3*S(CH3)2; 2.) 30percent H2O2/10percent NaOH / 1.) THF, 15 h, -10 deg C; 2.) 0 deg C to room temp., 3 h
6: 74 percent / pyridinium chloro-chromate / CH2Cl2 / 144 h / Ambient temperature
7: 1.) 1.6M n-C4H9Li/n-hexane / 1.) THF, 45 min; 2.) THF, 19 h, room temp.
With sodium hydroxide; n-butyllithium; hexane; dimethylsulfide borane complex; dihydrogen peroxide; nickel; sodium hydride; potassium carbonate; pyridinium chlorochromate; hydroquinone; In tetrahydrofuran; methanol; dichloromethane;
Guidance literature:
Multi-step reaction with 7 steps
1: 35 percent / hydroquinone / CH2Cl2 / 72 h / 6000480 Torr / Ambient temperature
2: 96 percent / K2CO3 / methanol / 20 h / Ambient temperature
3: 1.) NaH / 1.) DMF, 0 deg C, 1 h; 2.) 15 h
4: 98 percent / Raney-Nickel / tetrahydrofuran / 8 h / Ambient temperature
5: 1.) BH3*S(CH3)2; 2.) 30percent H2O2/10percent NaOH / 1.) THF, 15 h, -10 deg C; 2.) 0 deg C to room temp., 3 h
6: 74 percent / pyridinium chloro-chromate / CH2Cl2 / 144 h / Ambient temperature
7: 1.) 1.6M n-C4H9Li/n-hexane / 1.) THF, 45 min; 2.) THF, 19 h, room temp.
With sodium hydroxide; n-butyllithium; hexane; dimethylsulfide borane complex; dihydrogen peroxide; nickel; sodium hydride; potassium carbonate; pyridinium chlorochromate; hydroquinone; In tetrahydrofuran; methanol; dichloromethane;
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