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D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen phosphate)

Base Information Edit
  • Chemical Name:D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen phosphate)
  • CAS No.:165883-85-2
  • Molecular Formula:C41H81O19P3
  • Molecular Weight:971.004
  • Hs Code.:
  • Mol file:165883-85-2.mol
D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen phosphate)

Synonyms:D-myo-Inositol,1-[2,3-bis[(1-oxohexadecyl)oxy]propyl hydrogen phosphate] 3,4-bis(dihydrogenphosphate), (R)-

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Chemical Property of D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen phosphate) Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:995.9°C at 760 mmHg 
  • Flash Point:556.1°C 
  • PSA:332.00000 
  • Density:1.27g/cm3 
  • LogP:7.95830 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen phosphate)

There total 6 articles about D-myo-Inositol, 1-(2R)-2,3-bis(1-oxohexadecyl)oxypropyl hydrogen phosphate 3,4-bis(dihydrogen 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:
1D-O-(1,2-di-O-palmitoyl-sn-glycerol-3-O-methylphospho)-2,5,6-O-tris(methoxymethylene)-myo-inositol 3,4-bis(dibenzyl phosphate); With trimethylamine; at 20 ℃; for 36h;
With hydrogen; palladium on activated charcoal; In methanol; for 5h; atmospheric pressure;
With boron trifluoride diethyl etherate; ethanethiol; for 1h; Further stages.;
DOI:10.1021/jo0206418
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