Seselin

Base Information

Chemical Name:Seselin
CAS No.:523-59-1
Molecular Formula:C14H12O3
Molecular Weight:228.247
Hs Code.:2932999099
UNII:5634E8957P
DSSTox Substance ID:DTXSID60200322
Nikkaji Number:J11.874E
Wikidata:Q27104968
Metabolomics Workbench ID:46455
ChEMBL ID:CHEMBL71358
Mol file:523-59-1.mol

Synonyms:seselin

Suppliers and Price of Seselin

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

TRC
Seselin
10mg
$ 685.00

TRC
Seselin
5mg
$ 360.00

Cayman Chemical
Seselin
5mg
$ 375.00

Cayman Chemical
Seselin
1mg
$ 125.00

Arctom
Seselin ≥98%
10mg
$ 318.00

American Custom Chemicals Corporation
SESELIN 95.00%
5MG
$ 496.49

AK Scientific
Seselin
5mg
$ 606.00

Total 25 raw suppliers

Chemical Property of Seselin

Chemical Property:

Vapor Pressure:1.05E-06mmHg at 25°C
Melting Point:119-124 °C
Boiling Point:403°Cat760mmHg
Flash Point:170.5°C
PSA：39.44000
Density:1.222g/cm³
LogP:2.97720
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:228.078644241
Heavy Atom Count:17
Complexity:394

Purity/Quality:

99% ^*data from raw suppliers

Seselin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C
Uses Seselin is a coumarin compound that can be isolated from the root bark of the Citropsis articulata plant. Studies show that Seselin might exhibit potential antimalarial activity and that its derivatives may exhibit antithrombotic activity.

Technology Process of Seselin

There total 27 articles about Seselin 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: 94.0%

: 93-35-6
7-hydroxy-2H-chromen-2-one

: 1740-74-5
1,1-diethoxy-3-methyl-2-butene

: 523-59-1
seseline

Guidance literature:: With 3-Methylpyridine; at 100 ℃; for 0.333333h; Microwave irradiation;
DOI:10.1021/ol900444h

Reference yield: 85.0%

: 32268-30-7
2,4-dihydroxy-3-(3-methyl-2-but-en-1-yl)benzaldehyde

: 21204-67-1,2605-67-6
methyl (triphenylphosphoranylidene)acetate

: 523-59-1
seseline

Guidance literature:: 2,4-dihydroxy-3-(3-methyl-2-but-en-1-yl)benzaldehyde; With selenium bromide polystyrene resin; In dichloromethane; at 0 - 25 ℃; for 0.5h;

methyl (triphenylphosphoranylidene)acetate; With N,N-diethylaniline; at 165 ℃; for 3h;

With dihydrogen peroxide; In tetrahydrofuran; at 25 ℃; for 0.5h;
DOI:10.1002/(SICI)1521-3773(20000218)39:4<734::AID-ANIE734>3.0.CO;2-I