Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone

Base Information

Chemical Name:Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone
CAS No.:112100-07-9
Molecular Formula:C₇₂H₅₈N₂O₈
Molecular Weight:1079.26
Hs Code.:

Synonyms:BASF ROT300; KF 856; Lumogen F Red 300; Lumogen Red 300; Lumogen Red F 300;N,N'-Bis(2,6-diisopropylphenyl)-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxdiimide;ROT 300

Suppliers and Price of Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 31 raw suppliers

Chemical Property of Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone

Chemical Property:

PSA：0.00000
LogP:0.00000

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone

There total 5 articles about Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone 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:

: 81-33-4
3,4,9,10-perylene tetracarboxyxlic acid diimide

: 112100-07-9,123174-58-3
bis(2,6-diisopropylphenyl)-5,6,12,13-tetraphenoxyanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H, 9H)-tetraone

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / water / 4 h / 210 °C

2: bromine / 4 h / 80 - 145 °C

3: potassium hydroxide / water / 6 h / Reflux

4: acetic acid / water / 12 h / 100 °C

With sulfuric acid; bromine; acetic acid; potassium hydroxide; In water;

Reference yield:

: 24544-04-5
2,6-diisopropylbenzenamine

: 156028-26-1
1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride

: 112100-07-9,123174-58-3
bis(2,6-diisopropylphenyl)-5,6,12,13-tetraphenoxyanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H, 9H)-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1: propionic acid / 24 h / 140 °C

2: potassium carbonate / N,N-dimethyl-formamide / 24 h / 140 °C

With potassium carbonate; propionic acid; In N,N-dimethyl-formamide;

Reference yield:

: 156028-26-1
1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride

: 112100-07-9,123174-58-3
bis(2,6-diisopropylphenyl)-5,6,12,13-tetraphenoxyanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H, 9H)-tetraone

Guidance literature:: Multi-step reaction with 2 steps

1: propionic acid / 130 °C

2: 1-methyl-pyrrolidin-2-one; potassium carbonate / 90 °C / Inert atmosphere

With 1-methyl-pyrrolidin-2-one; potassium carbonate; propionic acid;
DOI:10.1002/chem.201604212