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5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone

Base Information
  • Chemical Name:5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone
  • CAS No.:94697-68-4
  • Molecular Formula:C9H14O6
  • Molecular Weight:218.207
  • Hs Code.:29322090
  • DSSTox Substance ID:DTXSID20662043
  • Nikkaji Number:J1.309.839E
  • Mol file:94697-68-4.mol
5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone

Synonyms:94697-68-4;5,6-O-Isopropylidene-L-gulono-1,4-lactone;(3S,4R,5S)-5-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-3,4-dihydroxydihydrofuran-2(3H)-one;(3S,4R,5S)-5-[(4S)-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-3,4-DIHYDROXYOXOLAN-2-ONE;5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone;SCHEMBL1738813;DTXSID20662043;JNTPPVKRHGNFKM-BNHYGAARSA-N;MFCD00077804;AKOS007930486;5,6-0-Isopropylidene-L-gulono-1,4-lactone;CS-0119989;5,6-isopropylidene-l-gulonic acid gamma-lactone;5,6-O-Isopropylidene-L-gulonic acid gamma-lactone;5,6-O-Isopropylidene-L-gluconic acid 1,4-lactone;5,6-O-Isopropylidene-L-gulonic acid gamma-lactone, >=99.0% (sum of enantiomers, TLC)

Suppliers and Price of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone
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
  • Usbiological
  • 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone
  • 1g
  • $ 355.00
  • Usbiological
  • 5,6-O-Isopropylidene-L-gulono-1,4-lactone
  • 1g
  • $ 333.00
  • TRC
  • 5,6-O-Isopropylidene-L-gulono-1,4-lactone
  • 2g
  • $ 145.00
  • Sigma-Aldrich
  • 5,6-O-Isopropylidene-L-gulonic acid γ-lactone ≥99.0% (sum of enantiomers, TLC)
  • 1g-f
  • $ 108.00
  • Sigma-Aldrich
  • 5,6-O-Isopropylidene-L-gulonic acid γ-lactone ≥99.0% (sum of enantiomers, TLC)
  • 1 g
  • $ 91.80
  • Sigma-Aldrich
  • 5,6-O-Isopropylidene-L-gulonic acid γ-lactone ≥99.0% (sum of enantiomers, TLC)
  • 5 g
  • $ 310.00
  • Sigma-Aldrich
  • 5,6-O-Isopropylidene-L-gulonic acid γ-lactone ≥99.0% (sum of enantiomers, TLC)
  • 5g-f
  • $ 365.00
  • Medical Isotopes, Inc.
  • 5,6-O-Isopropylidene-L-gulono-1,4-lactone
  • 5 g
  • $ 1480.00
  • Medical Isotopes, Inc.
  • 5,6-O-Isopropylidene-L-gulono-1,4-lactone
  • 1 g
  • $ 810.00
  • Biosynth Carbosynth
  • 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone
  • 10 g
  • $ 340.00
Total 16 raw suppliers
Chemical Property of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone
Chemical Property:
  • Melting Point:166-170 °C
     
  • Refractive Index:1.536 
  • PSA:85.22000 
  • LogP:-1.21490 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Methanol (Slightly), Water (Slightly) 
  • XLogP3:-1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:1
  • Exact Mass:218.07903816
  • Heavy Atom Count:15
  • Complexity:276
Purity/Quality:

98%, *data from raw suppliers

5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(OCC(O1)C2C(C(C(=O)O2)O)O)C
  • Isomeric SMILES:CC1(OC[C@H](O1)[C@@H]2[C@@H]([C@@H](C(=O)O2)O)O)C
  • Uses 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone is a useful starting material for the synthesis of an array of compounds modified in the 2 and 3 positions.
Technology Process of 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone

There total 11 articles about 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone 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 toluene-4-sulfonic acid; In tetrahydrofuran; DMF (N,N-dimethyl-formamide); water; at 0 - 20 ℃; for 18h;
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