1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-

Base Information

Chemical Name:1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-
CAS No.:77762-97-1
Molecular Formula:C₂₈H₃₀N₄O₄
Molecular Weight:486.571
Hs Code.:
NSC Number:353100
UNII:8IU5EE8ZMA
DSSTox Substance ID:DTXSID50228378
Nikkaji Number:J62.214A
Wikidata:Q83108361

Synonyms:8IU5EE8ZMA;77762-97-1;1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-;NSC-353100;NSC 353100;BRN 5673667;NSC353100;UNII-8IU5EE8ZMA;N,N'-Bis(4-piperidinobut-2-ynyl)-1,2,4,5-benzenetetracarboxylic 1,2:4,5-diimide;DTXSID50228378;2,6-BIS(4-(1-PIPERIDINYL)-2-BUTYNYL)BENZO(1,2-C:4,5-C')DIPYRROLE-1,3,5,7(2H,6H)-TETRONE;BENZO(1,2-C:4,5-C')DIPYRROLE-1,3,5,7(2H,6H)-TETRONE, 2,6-BIS(4-(1-PIPERIDINYL)-2-BUTYNYL)-

Suppliers and Price of 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-

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 2 raw suppliers

Chemical Property of 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-

Chemical Property:

Vapor Pressure:3.15E-18mmHg at 25°C
Boiling Point:677.8°C at 760 mmHg
Flash Point:295.7°C
Density:1.312g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:486.22670545
Heavy Atom Count:36
Complexity:922

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCN(CC1)CC#CCN2C(=O)C3=CC4=C(C=C3C2=O)C(=O)N(C4=O)CC#CCN5CCCCC5

Technology Process of 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)-

There total 2 articles about 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-diimide, N,N'-bis(4-(piperidino)but-2-ynyl)- 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: 35.0%

: 110-89-4
piperidine

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 18158-82-2
2,6-di-prop-2-ynyl-pyrrolo[3,4-f]isoindole-1,3,5,7-tetraone

: 77762-97-1
2,6-Bis-(4-piperidin-1-yl-but-2-ynyl)-pyrrolo[3,4-f]isoindole-1,3,5,7-tetraone

Guidance literature:: With copper(l) chloride; In 1,4-dioxane; for 3h; Heating;

Reference yield:

: 2550-73-4
pyrrolo[3,4-f]isoindole-1,3,5,7-tetraone

: 77762-97-1
2,6-Bis-(4-piperidin-1-yl-but-2-ynyl)-pyrrolo[3,4-f]isoindole-1,3,5,7-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium hydroxide, 65 percent alcohol / 1.) DMF, 1 h, r.t.; 2.) DMF, 70-80 deg C, 16 h

2: 35 percent / cuprous chloride / dioxane / 3 h / Heating

With potassium hydroxide; ethanol; copper(l) chloride; In 1,4-dioxane;