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ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside

Base Information Edit
  • Chemical Name:ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside
  • CAS No.:1259036-06-0
  • Molecular Formula:C25H32O9S
  • Molecular Weight:508.59
  • Hs Code.:
  • Mol file:1259036-06-0.mol
ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside

Synonyms:ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside

Suppliers and Price of ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside Edit
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Technology Process of ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside

There total 1 articles about ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside 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 dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃; for 3h;
DOI:10.1016/j.bmc.2012.04.017
Guidance literature:
With N-Bromosuccinimide; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.5h; Molecular sieve;
DOI:10.1016/j.tetlet.2011.04.060
Guidance literature:
ethylthio 4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranoside; With 4-(benzenesulfinyl)morpholine; trifluoromethylsulfonic anhydride; In dichloromethane; at -40 ℃; for 0.0833333h;
With water; sodium hydrogencarbonate; sodium thiosulfate; In dichloromethane;
With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/j.bmc.2012.04.017
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