Euparin

Base Information

Chemical Name:Euparin
CAS No.:532-48-9
Molecular Formula:C13H12 O3
Molecular Weight:216.236
Hs Code.:2932999099
UNII:46YA021ENM
DSSTox Substance ID:DTXSID40201256
Nikkaji Number:J11.686F
Wikidata:Q27135902
Metabolomics Workbench ID:139991
ChEMBL ID:CHEMBL503938
Mol file:532-48-9.mol

Synonyms:euparin

Suppliers and Price of Euparin

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

Crysdot
Euparin 95+%
5mg
$ 345.00

American Custom Chemicals Corporation
5-ACETYL-6-HYDROXY-2-ISOPROPENYLBENZOFURAN 95.00%
5MG
$ 496.65

Total 23 raw suppliers

Chemical Property of Euparin

Chemical Property:

Vapor Pressure:0.00857mmHg at 25°C
Melting Point:152-153℃
Refractive Index:1.4740 (estimate)
Boiling Point:258.3°Cat760mmHg
PKA:9.33±0.40(Predicted)
Flash Point:110°C
PSA：50.44000
Density:1.187g/cm³
LogP:3.37410
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:216.078644241
Heavy Atom Count:16
Complexity:310

Purity/Quality:

98% ^*data from raw suppliers

Euparin 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C

Technology Process of Euparin

There total 10 articles about Euparin 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: 82.0%

: 173992-05-7
5-acetyl-6-hydroxy-2-(1-hydroxy-1-methylethyl)benzofuran

: 532-48-9
1-(6-hydroxy-2-isopropenyl-benzofuran-5-yl)-ethanone

Guidance literature:: With boron tribromide; In dichloromethane; at -70 ℃; for 0.0833333h;

Reference yield: 32.0%

: 62069-33-4
1-(2,4-dihydroxy-5-iodophenyl)ethanone

: 56964-06-8
(3-methyl-3-buten-1-yn-1-yl)copper

: 532-48-9
1-(6-hydroxy-2-isopropenyl-benzofuran-5-yl)-ethanone

Guidance literature:: With pyridine; for 18h; Heating;

Reference yield:

: 89-84-9
2',4'-dihydroxy-4-acetophenone

: 532-48-9
1-(6-hydroxy-2-isopropenyl-benzofuran-5-yl)-ethanone

Guidance literature:: Multi-step reaction with 5 steps

1: silver trifluoroacetate,iodine / CHCl₃ / 1 h / 20 - 25 °C

2: 85 percent / K₂CO₃ / acetone / 0.75 h / Heating

3: 97 percent / PPh₃, CuI / PdCl₂ / triethylamine; dimethylformamide / 0.8 h / 80 °C

4: 88 percent / K₂CO₃ / methanol / 0.8 h / Heating

5: 82 percent / BBr₃ / CH₂Cl₂ / 0.08 h / -70 °C

With copper(l) iodide; silver trifluoroacetate; boron tribromide; potassium carbonate; triphenylphosphine; palladium dichloride; In methanol; dichloromethane; chloroform; triethylamine; N,N-dimethyl-formamide; acetone;