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Fuculose 1-phosphate

Base Information Edit
  • Chemical Name:Fuculose 1-phosphate
  • CAS No.:16562-58-6
  • Molecular Formula:C6H13O8P
  • Molecular Weight:244.138
  • Hs Code.:
  • DSSTox Substance ID:DTXSID301027442
  • Wikidata:Q27103634
  • Metabolomics Workbench ID:37693
  • Mol file:16562-58-6.mol
Fuculose 1-phosphate

Synonyms:fuculose 1-phosphate

Suppliers and Price of Fuculose 1-phosphate
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
Total 1 raw suppliers
Chemical Property of Fuculose 1-phosphate Edit
Chemical Property:
  • Vapor Pressure:5.83E-13mmHg at 25°C 
  • Boiling Point:519.4°Cat760mmHg 
  • Flash Point:267.9°C 
  • PSA:146.49000 
  • Density:1.75g/cm3 
  • LogP:-2.07680 
  • XLogP3:-3.2
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:2
  • Exact Mass:244.03480437
  • Heavy Atom Count:15
  • Complexity:264
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(C(C(O1)OP(=O)(O)O)O)O)O
  • Isomeric SMILES:C[C@H]1[C@H]([C@H]([C@@H](C(O1)OP(=O)(O)O)O)O)O
Technology Process of Fuculose 1-phosphate

There total 3 articles about Fuculose 1-phosphate 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:
Multi-step reaction with 2 steps
1: dimethylformamide / 0.17 h / 23 °C
In N,N-dimethyl-formamide;
DOI:10.1139/v90-165
Guidance literature:
Yield given. Multistep reaction;
DOI:10.1139/v90-165
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