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1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose

Base Information
  • Chemical Name:1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose
  • CAS No.:40690-74-2
  • Molecular Formula:C15H22O7
  • Molecular Weight:314.335
  • Hs Code.:
1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose

Synonyms:1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose

Suppliers and Price of 1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose
Supply Marketing:
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
  • Sigma-Aldrich
  • 3-O-Acryloyl-1,2:5,6-bis-O-isopropylidene-D-glucofuranose 99%
  • 1g
  • $ 184.00
Total 1 raw suppliers
Chemical Property of 1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose
Chemical Property:
  • Melting Point:76.9°C 
Purity/Quality:

98%,99%, *data from raw suppliers

3-O-Acryloyl-1,2:5,6-bis-O-isopropylidene-D-glucofuranose 99% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • General Description 1,2:5,6-Di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose (also referred to as 3-O-acryloyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranoside, AIGlc) is a sugar-derived acrylate monomer used in polymerization reactions, particularly in the synthesis of hyperbranched glycopolymers via controlled radical polymerization techniques such as atom transfer radical polymerization (ATRP). 1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose features an acrylate group at the C-3 position of a protected D-glucofuranose scaffold, enabling its incorporation into polymeric structures. After polymerization, the isopropylidene protecting groups can be removed to yield water-soluble glycopolymers with potential applications in biomaterials and ceramic technology. Additionally, it has been explored in asymmetric Baylis-Hillman reactions, though with moderate stereoselectivity.
Technology Process of 1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose

There total 9 articles about 1,2:5,6-di-O-isopropylidene-3-O-acrylate-α-D-glucopentoaldo-1,4-furanose 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; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1080/00304949909355350
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