Talosalate

Base Information

Chemical Name:Talosalate
CAS No.:66898-60-0
Molecular Formula:C17H12O6
Molecular Weight:312.2736
Hs Code.:

Synonyms:Talosalate (USAN/INN);Talosalate;Talosalatum [INN-Latin];Talosalato [INN-Spanish];Talosalatum;Talosalato;

Suppliers and Price of Talosalate

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
Talosalate
100mg
$ 180.00

American Custom Chemicals Corporation
TALOSALATE 95.00%
5MG
$ 502.85

Total 6 raw suppliers

Chemical Property of Talosalate

Chemical Property:

Vapor Pressure:4E-09mmHg at 25°C
Boiling Point:473.2°Cat760mmHg
Flash Point:211.2°C
PSA：78.90000
Density:1.4g/cm³
LogP:2.63790

Purity/Quality:

99% ^*data from raw suppliers

Talosalate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Talosalate is an inhibitor of blood platelet aggregation.

Technology Process of Talosalate

There total 4 articles about Talosalate 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: 89.0%

: 50-78-2,98201-60-6
aspirin

: 643-79-8
o-phthalic dicarboxaldehyde

: 66898-60-0
talosalate

Guidance literature:: With 3,5,3',5'-tetra-tert-butyl-4,4'-diphenoquinone; C₁₈H₁₂BrCl₃N₃O⁽¹⁺⁾*BF₄^(1-); potassium carbonate; lithium chloride; In chloroform; at -20 ℃; for 12h; enantioselective reaction; Catalytic behavior;
DOI:10.1038/s41467-019-09445-x

Reference yield: 54.0%

: 16859-59-9
3-hydroxy-1(3H)-isobenzofuranone

: 5663-67-2
2-acetoxybenzaldehyde

: 66898-60-0
3-oxo-1,3-dihydroisobenzofuran-1-yl 2-acetoxybenzoate

Guidance literature:: With 3,5,3',5'-tetra-tert-butyl-4,4'-diphenoquinone; BF₄^(1-)*C₁₈H₁₃Cl₃N₃O⁽¹⁺⁾; N-ethyl-N,N-diisopropylamine; In ethyl acetate; at 20 ℃; for 12h; enantioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/anie.201912926

Reference yield:

: 50-78-2,98201-60-6
aspirin

: 643-79-8
o-phthalic dicarboxaldehyde

: 66898-60-0
talosalate

: 66898-60-0
3-oxo-1,3-dihydroisobenzofuran-1-yl 2-acetoxybenzoate

Guidance literature:: With 3,5,3',5'-tetra-tert-butyl-4,4'-diphenoquinone; C₁₈H₁₂BrCl₃N₃O⁽¹⁺⁾*BF₄^(1-); potassium carbonate; lithium chloride; In dichloromethane; at 20 ℃; for 12h; Reagent/catalyst; Solvent; Overall yield = 92 %; enantioselective reaction;
DOI:10.1038/s41467-019-09445-x