2-benzyl-3-hydroxy-1-isoindolinone

Base Information

Chemical Name:2-benzyl-3-hydroxy-1-isoindolinone
CAS No.:17448-14-5
Molecular Formula:C15H13NO2
Molecular Weight:239.274
Hs Code.:
Mol file:17448-14-5.mol

Synonyms:3-hydroxy-2benzyl-2,3-dihydroisoindol-1-one;2-benzyl-3-hydroxyisoindolin-1-one;2-Benzyl-3-hydroxy-isoindolin-1-on;2-benzyl-3-hydroxy-2,3-dihydro-isoindol-1-one;

Suppliers and Price of 2-benzyl-3-hydroxy-1-isoindolinone

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

American Custom Chemicals Corporation
2-BENZYL-3-HYDROXY-1-ISOINDOLINONE 95.00%
5MG
$ 697.51

American Custom Chemicals Corporation
2-BENZYL-3-HYDROXY-1-ISOINDOLINONE 95.00%
10MG
$ 692.49

American Custom Chemicals Corporation
2-BENZYL-3-HYDROXY-1-ISOINDOLINONE 95.00%
1MG
$ 658.53

Total 0 raw suppliers

Chemical Property of 2-benzyl-3-hydroxy-1-isoindolinone

Chemical Property:

PSA：40.54000
LogP:2.27140

Purity/Quality:: 2-BENZYL-3-HYDROXY-1-ISOINDOLINONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-benzyl-3-hydroxy-1-isoindolinone

There total 16 articles about 2-benzyl-3-hydroxy-1-isoindolinone 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: 99.0%

: 2142-01-0
N-benzylphthalimide

: 17448-14-5
2-benzyl-3-hydroxy-2,3-dihydro-isoindol-1-one

Guidance literature:: With N,N,N,N,-tetramethylethylenediamine; Triethoxysilane; zinc(II) acetate dihydrate; In tetrahydrofuran; at 70 ℃; Reagent/catalyst; Solvent; regioselective reaction; Inert atmosphere;
DOI:10.1002/adsc.201400961