Saponarin

Base Information

Chemical Name:Saponarin
CAS No.:20310-89-8
Molecular Formula:C₂₇H₃₀O₁₅
Molecular Weight:594.526
Hs Code.:
European Community (EC) Number:805-140-3
UNII:3081Z76OX9
DSSTox Substance ID:DTXSID10174201
Nikkaji Number:J94.482C
Wikipedia:Saponarin
Wikidata:Q63408652
Metabolomics Workbench ID:68820
ChEMBL ID:CHEMBL4640510
Mol file:20310-89-8.mol

Synonyms:apigenin 6-C-glucosyl-7-O-glucoside;saponarin

Suppliers and Price of Saponarin

Supply Marketing:

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

Biorbyt Ltd
Saponarin
5 mg
$ 596.70

Biorbyt Ltd
Saponarin
10 mg
$ 778.60

AvaChem
Saponarin
20mg
$ 649.00

AvaChem
Saponarin
5mg
$ 249.00

AvaChem
Saponarin
1mg
$ 119.00

AvaChem
Saponarin
10mg
$ 349.00

Arctom
Saponarin ≥98%
10mg
$ 338.00

Arctom
Saponarin 98%
100mg
$ 2257.00

American Custom Chemicals Corporation
SAPONARIN 95.00%
5MG
$ 922.38

Total 25 raw suppliers

Chemical Property of Saponarin

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:228°C (dec.)
Boiling Point:919.5 °C at 760 mmHg
PKA:5.53±0.40(Predicted)
Flash Point:305.4 °C
PSA：260.20000
Density:1.723 g/cm³
LogP:-2.43520
XLogP3:-1.6
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:6
Exact Mass:594.15847025
Heavy Atom Count:42
Complexity:971

Purity/Quality:

≥98% ^*data from raw suppliers

Saponarin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O
Isomeric SMILES:C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)O)O

Technology Process of Saponarin

There total 7 articles about Saponarin 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: 87.0%

: 4',5-dibenzoyloxy-7-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-O-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyl)flavone

: 20310-89-8,72059-32-6
Saponarin

Guidance literature:: 4',5-dibenzoyloxy-7-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)-7-O-(2''',3''',4''',6'''-tetra-O-acetyl-β-D-glucopyranosyl)flavone; With sodium methylate; In tetrahydrofuran; methanol; at 20 ℃; for 3h;

In tetrahydrofuran; methanol;
DOI:10.1248/cpb.c13-00264

Reference yield:

: 7-acetoxy-4',5-dibenzoyloxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)flavone

: 20310-89-8,72059-32-6
Saponarin

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N,N',N'-tetramethylguanidine / acetonitrile / 3 h / 20 °C

2.1: silver (II) carbonate; quinoline / 0 - 20 °C / Inert atmosphere; Darkness

3.1: sodium methylate / methanol; tetrahydrofuran / 3 h / 20 °C

3.2: Dowex^? 50Wx8 (H⁺)

With quinoline; silver (II) carbonate; sodium methylate; N,N,N',N'-tetramethylguanidine; In tetrahydrofuran; methanol; acetonitrile; 2.1: |Koenigs-Knorr Glycosidation;
DOI:10.1248/cpb.c13-00264

Reference yield:

: 4',5-dibenzoyloxy-7-hydroxy-6-C-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranosyl)flavone

: 20310-89-8,72059-32-6
Saponarin

Guidance literature:: Multi-step reaction with 2 steps

1.1: silver (II) carbonate; quinoline / 0 - 20 °C / Inert atmosphere; Darkness

2.1: sodium methylate / methanol; tetrahydrofuran / 3 h / 20 °C

2.2: Dowex^? 50Wx8 (H⁺)

With quinoline; silver (II) carbonate; sodium methylate; In tetrahydrofuran; methanol; 1.1: |Koenigs-Knorr Glycosidation;
DOI:10.1248/cpb.c13-00264