CID 14334937

Base Information

Chemical Name:CID 14334937
CAS No.:63347-43-3
Molecular Formula:C22H20O10
Molecular Weight:444.395
Hs Code.:
Wikidata:Q105022102

Synonyms:Rothindin;3-(1,3-benzodioxol-5-yl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

Suppliers and Price of CID 14334937

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

Total 0 raw suppliers

Chemical Property of CID 14334937

Chemical Property:

Vapor Pressure:4.77E-22mmHg at 25°C
Boiling Point:724.8°Cat760mmHg
Flash Point:256.8°C
Density:1.601g/cm³
XLogP3:0.8
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:4
Exact Mass:444.10564683
Heavy Atom Count:32
Complexity:728

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O

Technology Process of CID 14334937

There total 4 articles about CID 14334937 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: 92.0%

: 58528-02-2
rothindin tetraacetate

: 63347-43-3
pseudobaptigenin 7‐O‐β‐D‐glucoside

Guidance literature:: With zinc diacetate; In methanol; for 7h; Heating;
DOI:10.1081/SCC-100106200

Reference yield:

: 90-29-9
7-hydroxy-3',4'-methylenedioxyisoflavone

: 63347-43-3
pseudobaptigenin 7‐O‐β‐D‐glucoside

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / K₂CO₃; dodecyltrimethylammonium bromide / acetone; dimethylformamide / 5 h / Heating

2: 92 percent / Zn(OAc)2 / methanol / 7 h / Heating

With zinc diacetate; dodecyltrimethylammonium bromide; potassium carbonate; In methanol; N,N-dimethyl-formamide; acetone;
DOI:10.1081/SCC-100106200

Reference yield:

: 572-09-8,3068-32-4,4026-32-8,6919-96-6,13242-53-0,14227-54-4,14795-18-7,19186-59-5,19285-38-2,21698-13-5,29907-26-4,53369-42-9,60619-58-1,61303-35-3,67337-79-5,69127-37-3,70749-15-4,72002-90-5,75247-30-2,75880-74-9,78418-57-2,102339-89-9,102339-90-2,103530-40-1,114028-03-4,114718-45-5,138514-70-2,138514-71-3
2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide

: 63347-43-3
pseudobaptigenin 7‐O‐β‐D‐glucoside

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / K₂CO₃; dodecyltrimethylammonium bromide / acetone; dimethylformamide / 5 h / Heating

2: 92 percent / Zn(OAc)2 / methanol / 7 h / Heating

With zinc diacetate; dodecyltrimethylammonium bromide; potassium carbonate; In methanol; N,N-dimethyl-formamide; acetone;
DOI:10.1081/SCC-100106200