1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro-

Base Information

Chemical Name:1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro-
CAS No.:864867-11-8
Molecular Formula:C13H14BrNO
Molecular Weight:280.164
Hs Code.:2933998090

Synonyms:5-bromo-2-cyclopentyl-1-oxo-isoindoline;5-bromo-2-cyclopentylisoindolin-1-one;1H-Isoindol-1-one,5-bromo-2-cyclopentyl-2,3-dihydro;5-bromo-2-cyclopentyl-2,3-dihydroisoindol-1-one;

Suppliers and Price of 1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro-

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

SynQuest Laboratories
5-Bromo-2-cyclopentylisoindolin-1-one
250 mg
$ 384.00

Matrix Scientific
5-Bromo-2-cyclopentylisoindolin-1-one
1g
$ 1126.00

Total 1 raw suppliers

Chemical Property of 1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro-

Chemical Property:

PSA：20.31000
LogP:3.28540

Purity/Quality:: 5-Bromo-2-cyclopentylisoindolin-1-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro-

There total 4 articles about 1H-Isoindol-1-one, 5-bromo-2-cyclopentyl-2,3-dihydro- 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:

: 99548-55-7
4-bromo-2-methyl-benzoic acid methyl ester

: 864867-11-8
5-bromo-2-cyclopentyl-2,3-dihydro-1H-isoindol-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 12 h / 68 °C / Inert atmosphere

2: potassium carbonate / acetonitrile / 12 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; In tetrachloromethane; acetonitrile;
DOI:10.1021/jm3005306

Reference yield:

: 1003-03-8
Cyclopentamine

: 78471-43-9
methyl 4-bromo-2-(bromomethyl)benzoate

: 864867-11-8
5-bromo-2-cyclopentyl-2,3-dihydro-1H-isoindol-1-one

Guidance literature:: With potassium carbonate; In acetonitrile; for 12h; Inert atmosphere; Reflux;
DOI:10.1021/jm3005306

Reference yield:

: 68837-59-2
4-bromo-2-methylbenzoic acid

: 864867-11-8
5-bromo-2-cyclopentyl-2,3-dihydro-1H-isoindol-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / 12 h / Reflux; Inert atmosphere

2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 12 h / 68 °C / Inert atmosphere

3: potassium carbonate / acetonitrile / 12 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sulfuric acid; potassium carbonate; In tetrachloromethane; acetonitrile;
DOI:10.1021/jm3005306