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Pro-xylane

Base Information
  • Chemical Name:Pro-xylane
  • CAS No.:439685-79-7
  • Molecular Formula:C8H16O5
  • Molecular Weight:192.212
  • Hs Code.:
  • UNII:4U3GMG1OT1
  • ChEMBL ID:CHEMBL479843
  • DSSTox Substance ID:DTXSID10196004
  • Metabolomics Workbench ID:153987
  • Nikkaji Number:J2.377.592A
  • Wikidata:Q27260499
Pro-xylane

Synonyms:C-beta-D-xylopyranoside-2-hydroxypropane;C-xylopyranoside-2-hydroxypropane;C-xyloside;pro-xylane

Suppliers and Price of Pro-xylane
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 108 raw suppliers
Chemical Property of Pro-xylane
Chemical Property:
  • XLogP3:-1.8
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:192.09977361
  • Heavy Atom Count:13
  • Complexity:163
Purity/Quality:

98%,30%,50% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(CC1C(C(C(CO1)O)O)O)O
  • Isomeric SMILES:CC(C[C@H]1[C@@H]([C@H]([C@@H](CO1)O)O)O)O
  • Recent ClinicalTrials:Transcriptomic Study of ER 4017 Topical Application in Elderly Subject
Technology Process of Pro-xylane

There total 7 articles about Pro-xylane 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 tris(acetoxy)borohydride; In isopropyl alcohol; at 20 ℃; Product distribution / selectivity;
Guidance literature:
With 10 wt% Pd(OH)2 on carbon; hydrogen; In ethyl acetate; at 20 ℃; under 620.594 Torr; Schlenk technique;
Guidance literature:
With sodium tris(acetoxy)borohydride; In isopropyl alcohol;
DOI:10.1016/j.bmcl.2008.12.037
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