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2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside

Base Information Edit
  • Chemical Name:2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside
  • CAS No.:121063-56-7
  • Molecular Formula:C12H18O8
  • Molecular Weight:290.27
  • Hs Code.:
  • Mol file:121063-56-7.mol
2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside

Synonyms:

Suppliers and Price of 2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2,5-Dimethyl-4-hydroxy-3(2H)-furanoneβ-D-Glucopyranoside(MixtureofDiastereomers)
  • 100mg
  • $ 1390.00
  • TRC
  • 2,5-Dimethyl-4-hydroxy-3(2H)-furanoneβ-D-Glucopyranoside(MixtureofDiastereomers)
  • 10mg
  • $ 180.00
Total 2 raw suppliers
Chemical Property of 2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside Edit
Chemical Property:
  • Melting Point:>47°C (dec.) 
  • Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere 
  • Solubility.:Methanol (Slightly), Water (Slightly) 
Purity/Quality:

99% *data from raw suppliers

2,5-Dimethyl-4-hydroxy-3(2H)-furanoneβ-D-Glucopyranoside(MixtureofDiastereomers) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2,5-Dimethyl-4-hydroxy-3(2H)-furanone β-D-Glucopyranoside is the glucopyranoside analogue of 2,5-Dimethyl-4-hydroxy-3(2H)-furanone and a component of strawberry fruits.
Technology Process of 2,5-dimethyl-4-hydroxy-3(2H)-furanone β-D-glucopyranoside

There total 5 articles about 2,5-dimethyl-4-hydroxy-3(2H)-furanone 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 sodium methylate; In methanol; for 4h; Ambient temperature;
DOI:10.1016/0031-9422(89)80068-8
Guidance literature:
With sodium carbonate; In methanol; at 20 ℃; for 4h;
DOI:10.1081/CAR-120019010
Guidance literature:
Multi-step reaction with 2 steps
1: 19 percent / tetrabutylammonium bromide; aqueous sodium hydroxide / CH2Cl2 / 0.75 h / 35 °C
2: 50 percent / sodium carbonate / methanol / 4 h / 20 °C
With sodium hydroxide; tetrabutylammomium bromide; sodium carbonate; In methanol; dichloromethane;
DOI:10.1081/CAR-120019010
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