2-(4-Acetylphenyl)isoindolin-1-one

Base Information

Chemical Name:2-(4-Acetylphenyl)isoindolin-1-one
CAS No.:60025-40-3
Molecular Formula:C16H13NO2
Molecular Weight:251.285
Hs Code.:
DSSTox Substance ID:DTXSID30358703
Nikkaji Number:J699.058D
Wikidata:Q82139478

Synonyms:2-(4-acetylphenyl)isoindolin-1-one;60025-40-3;1H-Isoindol-1-one, 2-(4-acetylphenyl)-2,3-dihydro-;2-(4-acetylphenyl)-3H-isoindol-1-one;SCHEMBL688977;F1172-0025;DTXSID30358703;GPQDDMWXQCKJCQ-UHFFFAOYSA-N;STL321914;AKOS005137151;CCG-274882;SR-01000010658;2-(4-acetylphenyl)-2,3-dihydro-1H-isoindol-1-one;SR-01000010658-1;2-(4-acetylphenyl)-2,3-dihydro-1H-isoindole-1-one;2-(4-acetylphenyl)-2,3-dihydro-lH-isoindole-1-one

Suppliers and Price of 2-(4-Acetylphenyl)isoindolin-1-one

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-(4-ACETYL-PHENYL)-2,3-DIHYDRO-ISOINDOL-1-ONE 95.00%
5MG
$ 501.66

Total 0 raw suppliers

Chemical Property of 2-(4-Acetylphenyl)isoindolin-1-one

Chemical Property:

Melting Point:238-239 °C(Solv: chloroform (67-66-3); ethanol (64-17-5))
Boiling Point:468.5±45.0 °C(Predicted)
PSA：37.38000
Density:1.245±0.06 g/cm3(Predicted)
LogP:3.11460
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:251.094628657
Heavy Atom Count:19
Complexity:371

Purity/Quality:: 2-(4-ACETYL-PHENYL)-2,3-DIHYDRO-ISOINDOL-1-ONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC=C(C=C1)N2CC3=CC=CC=C3C2=O

Technology Process of 2-(4-Acetylphenyl)isoindolin-1-one

There total 11 articles about 2-(4-Acetylphenyl)isoindolin-1-one 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: 92.0%

: 99-92-3
p-aminobenzophenone

: 119-67-5
o-carboxybenzaldehyde

: 60025-40-3
2-(4-acetylphenyl)-2,3-dihydro-1H-isoindole-1-one

Guidance literature:: With aluminum (III) chloride; In ethanol; at 70 ℃; for 12h; chemoselective reaction;
DOI:10.1039/c2gc36305d

Reference yield: 90.0%

: 99-92-3
p-aminobenzophenone

: 7115-91-5
2-ethoxycarbonylbenzyl bromide

: 60025-40-3
2-(4-acetylphenyl)-2,3-dihydro-1H-isoindole-1-one

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃;
DOI:10.1515/HC.2002.8.3.281

Reference yield: 84.0%

: 99-92-3
p-aminobenzophenone

: 643-79-8
o-phthalic dicarboxaldehyde

: 60025-40-3
2-(4-acetylphenyl)-2,3-dihydro-1H-isoindole-1-one

Guidance literature:: With 1,2,3-Benzotriazole; 2-hydroxyethanethiol; In acetonitrile; at 20 ℃; for 13h; pH=9.6; Inert atmosphere;
DOI:10.3987/COM-15-S(T)38