2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

Base Information

Chemical Name:2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione
CAS No.:1128-13-8
Molecular Formula:C6H8N4O2
Molecular Weight:168.155
Hs Code.:
DSSTox Substance ID:DTXSID10509655
Wikidata:Q82367397

Synonyms:1128-13-8;2,3,5,6-tetraaminobenzoquinone;2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione;2,5-Cyclohexadiene-1,4-dione, 2,3,5,6-tetraamino-;tetraamino-p-benzoquinone;Tetraamino-1,4-benzoquinone;YSZC821;SCHEMBL1254805;DTXSID10509655;DNHCPEFCQYRQQN-UHFFFAOYSA-N;AKOS028112226;2,3,5,6-tetraamino-1,4-benzoquinone;BS-46767;CS-0170336;E75615;2,5-Cyclohexadiene-1,4-dione,2,3,5,6-tetraamino-;InChI=1/C6H8N4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11/h7-10H

Suppliers and Price of 2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

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
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price

Total 19 raw suppliers

Chemical Property of 2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

Chemical Property:

XLogP3:-1.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:0
Exact Mass:168.06472551
Heavy Atom Count:12
Complexity:278

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1(=C(C(=O)C(=C(C1=O)N)N)N)N

Technology Process of 2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione

There total 9 articles about 2,3,5,6-Tetraaminocyclohexa-2,5-diene-1,4-dione 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: 88.0%

: 118-75-2
chloranil

: 1128-13-8
2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

Guidance literature:: chloranil; With potassium phtalimide; In acetonitrile; for 18h; Reflux; Inert atmosphere;

With hydrazine hydrate; at 20 - 80 ℃; for 3h; Inert atmosphere;
DOI:10.1002/chem.201900879

Reference yield: 88.0%

: 99054-61-2
2,3,5,6-tetraphthalimido-1,4-benzoquinone

: 1128-13-8
2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

Guidance literature:: With hydrazine hydrate; at 20 - 80 ℃; for 4h;
DOI:10.1002/chem.201900002

Reference yield:

: 7210-71-1
2,5-dichloro-3,6-dimethoxy-1,4-benzoquinone

: 1128-13-8
2,3,5,6-tetraaminocyclohexa-2,5-diene-1,4-dione

Guidance literature:: Multi-step reaction with 2 steps

1: NaN₃ / methanol

2: (i) NH₃, EtOH, (ii) aq. Na₂S₂O₄, NaOH, (iii) O₂

With sodium azide; In methanol;
DOI:10.1016/S0040-4020(01)82792-7