Neodiosmin

Base Information

• Chemical Name: Neodiosmin
• CAS No.: 38665-01-9
• Molecular Formula: C28H32 O15
• Molecular Weight: 608.553
• Hs Code.: 2938900000
• Metabolomics Workbench ID: 74675
• Mol file: 38665-01-9.mol

Synonyms:Neodiosmin;Diosmetin-7-neohesperidoside;7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one;Diosmetin-7-O-neohesperidoside;7-[[2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one;BCP07307;NS00015835

Chemical Property of Neodiosmin

Chemical Property:

• Melting Point: 187～192℃
• Boiling Point: 930.4±65.0 °C(Predicted)
• PKA: 6.08±0.40(Predicted)
• PSA: 238.20000
• Density: 1.68±0.1 g/cm3(Predicted)
• LogP: -1.08970
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: -0.3
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 7
• Exact Mass: 608.17412031
• Heavy Atom Count: 43
• Complexity: 995

Purity/Quality:

98% ^*data from raw suppliers

Neodiosmin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O
• Uses: Neodiosmin is a flavone glycoside isolated from C. aurantium. Neodiosmin along with other citrus flavonoids showed antiproliferative activities against several tumor and normal human cell lines.

Technology Process of Neodiosmin

There total 1 articles about Neodiosmin 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: 72.0%

neohesperidin (13241-33-3,61303-28-4,61303-29-5,61303-30-8,61347-97-5,61348-24-1,88294-38-6,139686-38-7) → 4′-O-methylluteolin-7-O-rhamnoglucoside (38665-01-9)

Guidance literature:

With iodine; In pyridine; at 90 ℃; for 8h;

DOI:10.1002/ardp.19833160307

upstream raw materials:

neohesperidin

Refernces