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1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose

Base Information
  • Chemical Name:1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose
  • CAS No.:15080-25-8
  • Molecular Formula:C12H20O6
  • Molecular Weight:260.287
  • Hs Code.:
  • NSC Number:170231
  • Nikkaji Number:J3.275.000A
  • Wikidata:Q105178481
1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose

Synonyms:20880-93-7;25018-67-1;1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose;NSC170231;NFHXOQDPQIQPKT-UHFFFAOYSA-N;NSC-170231;15080-25-8;FT-0638485;FT-0773342;J-011805;alpha-D-Fructopyranose, 1,2:4,5-bis-O-(1-methylethylidene)-;Fructopyranose, 1,2:4,5-di-O-isopropylidene-, .alpha.-D-;2,2,2',2'-Tetramethylspiro[tetrahydro-4H-1,3-dioxolo[4,5-c]pyran-6,4'-[1,3]dioxolane]-7-ol

Suppliers and Price of 1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose
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
Total 1 raw suppliers
Chemical Property of 1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose
Chemical Property:
  • XLogP3:-0.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:260.12598835
  • Heavy Atom Count:18
  • Complexity:355
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1(OCC2(O1)C(C3C(CO2)OC(O3)(C)C)O)C
Technology Process of 1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose

There total 9 articles about 1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose 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 sulfuric acid; sodium hydroxide; at 0 - 50 ℃; Further stages;
DOI:10.1002/mabi.201600529
Guidance literature:
With toluene-4-sulfonic acid; In acetone; at -20 - 5 ℃;
DOI:10.1055/s-0033-1340825
upstream raw materials:

2,2-dimethoxy-propane

D-fructose

acetone

L-fructose

Downstream raw materials:

Shi's ketone

C31H26N2O9

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