N-propoxyphthalimide

Base Information

Chemical Name:N-propoxyphthalimide
CAS No.:51951-26-9
Molecular Formula:C11H11NO3
Molecular Weight:205.21000
Hs Code.:
DSSTox Substance ID:DTXSID00377668
Nikkaji Number:J1.805.229F
Wikidata:Q82166976
Mol file:51951-26-9.mol

Synonyms:N-propoxyphthalimide;51951-26-9;2-Propoxyisoindoline-1,3-dione;2-propoxyisoindole-1,3-dione;2-propoxy-1H-isoindole-1,3(2H)-dione;SCHEMBL6625137;DTXSID00377668;WEXGSEQUJOCZRR-UHFFFAOYSA-N;MFCD00231454;STK407696;AKOS002684630;SB65705;2-propoxy-2,3-dihydro-1H-isoindole-1,3-dione;12H-934

Suppliers and Price of N-propoxyphthalimide

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-PROPOXY-1H-ISOINDOLE-1,3(2H)-DIONE 95.00%
5MG
$ 697.51

American Custom Chemicals Corporation
2-PROPOXY-1H-ISOINDOLE-1,3(2H)-DIONE 95.00%
10MG
$ 692.49

American Custom Chemicals Corporation
2-PROPOXY-1H-ISOINDOLE-1,3(2H)-DIONE 95.00%
1MG
$ 658.53

Total 3 raw suppliers

Chemical Property of N-propoxyphthalimide

Chemical Property:

PSA：46.61000
LogP:1.56210
XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:205.07389321
Heavy Atom Count:15
Complexity:253

Purity/Quality:

99% ^*data from raw suppliers

2-PROPOXY-1H-ISOINDOLE-1,3(2H)-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCON1C(=O)C2=CC=CC=C2C1=O

Technology Process of N-propoxyphthalimide

There total 6 articles about N-propoxyphthalimide 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: 98.0%

: 71-23-8
propan-1-ol

: 524-38-9
N-hydroxyphthalimide

: 51951-26-9
N-propoxyphthalimide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; for 16h; Ambient temperature;
DOI:10.1021/jm9607921

Reference yield: 89.0%

: 524-38-9
N-hydroxyphthalimide

: 107-08-4
1-iodo-propane

: 51951-26-9
N-propoxyphthalimide

Guidance literature:: N-hydroxyphthalimide; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.5h; Inert atmosphere;

1-iodo-propane; In N,N-dimethyl-formamide; mineral oil; at 70 ℃; for 3.5h; Inert atmosphere;
DOI:10.1016/j.tet.2016.08.060