p-broMoxylylphthaliMide

Base Information

Chemical Name:p-broMoxylylphthaliMide
CAS No.:101367-16-2
Molecular Formula:C16H12BrNO2
Molecular Weight:330.181
Hs Code.:
Mol file:101367-16-2.mol

Synonyms:2-{[4-(bromomethyl)phenyl]methyl}-1H-isoindole-1,3(2H)-dione;2-[4-(bromomethyl)benzyl]isoindoline-1,3-dione;4-phthalimidomethylbenzyl bromide;2-(4-Bromomethyl-benzyl)-isoindole-1,3-dione;2-(4-(bromomethyl)benzyl)isoindoline-1,3-dione;

Suppliers and Price of p-broMoxylylphthaliMide

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

Total 1 raw suppliers

Chemical Property of p-broMoxylylphthaliMide

Chemical Property:

PSA：37.38000
LogP:3.31560

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of p-broMoxylylphthaliMide

There total 7 articles about p-broMoxylylphthaliMide 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: 63.0%

: 623-24-5
1,4-bis(bromomethyl)benzene

: 136918-14-4,85-41-6
phthalimide

: 101367-16-2
2-{[4-(bromomethyl)phenyl]methyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In acetonitrile; at 25 ℃; for 18h; Inert atmosphere;
DOI:10.1039/c7ob02347b

Reference yield: 60.0%

: 439691-95-9
2-(4-(hydroxymethyl)benzyl)isoindoline-1,3-dione

: 101367-16-2
2-{[4-(bromomethyl)phenyl]methyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 25 ℃;

Reference yield: 32.0%

: 623-24-5
1,4-bis(bromomethyl)benzene

: 136918-14-4,85-41-6
phthalimide

: 30391-55-0
α,α-4-bis(1H-isoindol-1,3(2H)-dione)xylene

: 101367-16-2
2-{[4-(bromomethyl)phenyl]methyl}-1H-isoindole-1,3(2H)-dione

Guidance literature:: phthalimide; With potassium carbonate; for 1h; Milling;

1,4-bis(bromomethyl)benzene; In N,N-dimethyl-formamide; for 1h; regioselective reaction; Milling;
DOI:10.3762/bjoc.13.169