CAS 160549-11-1: 2-Deoxy-3,4,6-tris-O-(phenylmethyl)-<span class="text-smallcaps">D</span>-arabino-hexopyranose
Formula:C27H30O5
InChI:InChI=1S/C27H30O5/c28-26-16-24(30-18-22-12-6-2-7-13-22)27(31-19-23-14-8-3-9-15-23)25(32-26)20-29-17-21-10-4-1-5-11-21/h1-15,24-28H,16-20H2/t24-,25-,26?,27+/m1/s1
InChI key:InChIKey=PDGHLARNGSMEJE-GWDBROLASA-N
SMILES:O(CC1=CC=CC=C1)[C@H]2[C@H](OCC3=CC=CC=C3)CC(O)O[C@@H]2COCC4=CC=CC=C4
Synonyms:- D-arabino-Hexopyranose, 2-deoxy-3,4,6-tris-O-(phenylmethyl)-
- 2-Deoxy-3,4,6-tris-O-(phenylmethyl)-D-arabino-hexopyranose
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Found 4 products.
(4R,5S,6R)-4,5-bis(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol
CAS:Purity:98%Molecular weight:434.5320129394531(4R,5S,6R)-4,5-Bis(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol
CAS:(4R,5S,6R)-4,5-Bis(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-ol is a flavonoid that has been found to have anti-inflammatory properties. This compound was synthesized by the reaction of (4R,5S,6R)-4,5-bis(benzyloxy)tetrahydro-2H-pyran with benzyl bromide and acetone. The synthesis was done in two steps: first the reaction between acetone and benzyl bromide gave an intermediate which underwent a second reaction with tetrahydropyran to give the desired product. The mechanistic study of this compound revealed it to be a competitive inhibitor of cyclooxygenase enzymes. It is also shown to inhibit the production of nitric oxide from peroxynitrite inFormula:C27H30O5Purity:Min. 95%Molecular weight:434.5 g/molRef: 3D-KGA54911
Discontinued product3,4,6-Tri-O-benzyl-2-deoxy-D-glucopyranose
CAS:Formula:C27H30O5Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:434.53
