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3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium

Base Information
  • Chemical Name:3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium
  • CAS No.:1432064-40-8
  • Molecular Formula:C55H73O12S*Na
  • Molecular Weight:981.233
  • Hs Code.:
3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium

Synonyms:

Suppliers and Price of 3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium
Chemical Property:
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MSDS Files:
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Technology Process of 3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium

There total 8 articles about 3-O-(6-deoxy-6-sulfo-α-D-glucopyranosyl)-1,2-di-O-6-(4'-pentyl-[1,1'-biphenyl]-4-yl)hexanoylglycerol sodium 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 20% palladium hydroxide-activated charcoal; hydrogen; In ethanol; at 20 ℃; for 16h;
DOI:10.1002/chem.201203296
Guidance literature:
Multi-step reaction with 4 steps
1: AD-mix-α / tert-butyl alcohol; water / 22 h / 20 °C
2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 20 h / 20 °C
3: acetic acid; Oxone; potassium acetate / 16 h / 20 °C
4: 20% palladium hydroxide-activated charcoal; hydrogen / ethanol / 16 h / 20 °C
With dmap; Oxone; AD-mix-α; 20% palladium hydroxide-activated charcoal; hydrogen; potassium acetate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1002/chem.201203296
Guidance literature:
Multi-step reaction with 2 steps
1: acetic acid; Oxone; potassium acetate / 16 h / 20 °C
2: 20% palladium hydroxide-activated charcoal; hydrogen / ethanol / 16 h / 20 °C
With Oxone; 20% palladium hydroxide-activated charcoal; hydrogen; potassium acetate; acetic acid; In ethanol;
DOI:10.1002/chem.201203296
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