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Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure

Base Information
  • Chemical Name:Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure
  • CAS No.:119437-89-7
  • Molecular Formula:C50H56O14
  • Molecular Weight:880.986
  • Hs Code.:
Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure

Synonyms:Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure
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Technology Process of Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure

There total 10 articles about Benzyl-5-O-(3,4,6,7-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranosyl)-3-desoxy-2-octulopyranosylonsaeure 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 sodium hydroxide; In methanol; water; for 2h; Ambient temperature;
Guidance literature:
Multi-step reaction with 9 steps
1: 1.) silver silicate / 1.) CH2Cl2, 1 h, 2.) CH2Cl2, 48 h, from -78 deg C to RT
2: 1.) 0.1 M NaOMe, 2.) imidazole / 1.) MeOH, 2 h, RT, 2.) DMF, 5 min, -10 deg C
4: 1.) silver triflate / 1.) CH2Cl2, 1 h, 2.) CH2Cl2, 60 h, from -40 to -15 deg C
5: 1.) H2, (1,5-cyclooctadien)iridium(I) hexafluorophosphate, 2.) I2 / 1.) THF, 15 min, RT, 2.) THF, H2O, 10 min
6: 1 M Bu4NF/THF / 0.25 h / -10 °C
7: 100 mg / pyridine, DMAP / 8 h / Ambient temperature
8: 98 percent / 0.1 M NaOMe / methanol / 2 h / Ambient temperature
9: 98 percent / 1 N NaOH / methanol; H2O / 2 h / Ambient temperature
With tetrahydrofuran; pyridine; 1H-imidazole; dmap; sodium hydroxide; (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate; silver silicate; tetrabutyl ammonium fluoride; hydrogen; iodine; sodium methylate; silver trifluoromethanesulfonate; In methanol; water;
Guidance literature:
Multi-step reaction with 7 steps
2: 1.) silver triflate / 1.) CH2Cl2, 1 h, 2.) CH2Cl2, 60 h, from -40 to -15 deg C
3: 1.) H2, (1,5-cyclooctadien)iridium(I) hexafluorophosphate, 2.) I2 / 1.) THF, 15 min, RT, 2.) THF, H2O, 10 min
4: 1 M Bu4NF/THF / 0.25 h / -10 °C
5: 100 mg / pyridine, DMAP / 8 h / Ambient temperature
6: 98 percent / 0.1 M NaOMe / methanol / 2 h / Ambient temperature
7: 98 percent / 1 N NaOH / methanol; H2O / 2 h / Ambient temperature
With tetrahydrofuran; pyridine; dmap; sodium hydroxide; (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate; tetrabutyl ammonium fluoride; hydrogen; iodine; sodium methylate; silver trifluoromethanesulfonate; In methanol; water;
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