10-Hydroxyoleuropein

Base Information

• Chemical Name: 10-Hydroxyoleuropein
• CAS No.: 84638-44-8
• Molecular Formula: C25H32 O14
• Molecular Weight: 556.521
• Nikkaji Number: J398.959C
• Wikidata: Q104397193

Synonyms:10-hydroxyl-oleuropein;10-hydroxyoleuropein

Chemical Property of 10-Hydroxyoleuropein

Chemical Property:

• Vapor Pressure: 1.37E-28mmHg at 25°C
• Boiling Point: 821.9°Cat760mmHg
• Flash Point: 273.3°C
• Density: 1.55g/cm³
• XLogP3: -1.7
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 14
• Rotatable Bond Count: 12
• Exact Mass: 556.17920569
• Heavy Atom Count: 39
• Complexity: 890

Purity/Quality:

98.0% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O
• Isomeric SMILES: COC(=O)C1=CO[C@H](/C(=C/CO)/[C@@H]1CC(=O)OCCC2=CC(=C(C=C2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O

Technology Process of 10-Hydroxyoleuropein

There total 2 articles about 10-Hydroxyoleuropein 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:

Reference yield:

(4S,6S)-4-[2-(3,4-Dihydroxy-phenyl)-ethoxycarbonylmethyl]-5-[2-hydroxy-eth-(E)-ylidene]-6-{(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(E)-3-(4-hydroxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-2-yloxy}-5,6-dihydro-4H-pyran-3-carboxylic acid methyl ester → 10-hydroxy-oleuropein (84638-44-8)

Guidance literature:

With sodium carbonate; In methanol; at 40 ℃; for 3h;

DOI:10.1016/S0031-9422(97)00790-5

Reference yield:

C34H38O17 → 10-hydroxy-oleuropein (84638-44-8)

Guidance literature:

With sodium carbonate; In methanol; at 40 ℃; for 3h;

DOI:10.1016/S0031-9422(97)00790-5

Reference yield:

10-hydroxy-oleuropein (84638-44-8) → C19H22O9 (125339-16-4)

Guidance literature:

With β-glucosidase; at 37 ℃; for 12h; pH=5.2; aq. acetate buffer; Enzymatic reaction;

DOI:10.1016/j.phytochem.2009.09.009

Downstream raw materials:

C₁₉H₂₂O₉

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