Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-

Base Information

• Chemical Name: Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-
• CAS No.: 55510-03-7
• Molecular Formula: C4H2 N8 O10
• Molecular Weight: 322.107
• European Community (EC) Number: 259-682-5
• DSSTox Substance ID: DTXSID7069029
• Wikidata: Q4456641
• Mol file: 55510-03-7.mol

Synonyms:55510-03-7;EINECS 259-682-5;Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-;Tetranitroglycoluril;Imidazo(4,5-d)imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-;Tetrahydro-1,3,4,6-tetranitroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione;Tetrahydro-1,3,4,6-tetranitroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione;DTXSID7069029;SCHEMBL17643383;C4H2N8O10;C4-H2-N8-O10;Q4456641

Chemical Property of Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-

Chemical Property:

• Vapor Pressure: 8.1E-17mmHg at 25°C
• Boiling Point: 650.8°C at 760 mmHg
• Flash Point: 347.4°C
• PSA: 230.38000
• Density: 2.51g/cm³
• LogP: -0.27500
• XLogP3: -0.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 0
• Exact Mass: 321.98938829
• Heavy Atom Count: 22
• Complexity: 506

Purity/Quality:

99% ^*data from raw suppliers

TETRAHYDRO-1,3,4,6-TETRANITROIMIDAZO[4,5-D]IMIDAZOLE-2,5(1H,3H)-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Uses -> Explosives
• Canonical SMILES: C12C(N(C(=O)N1[N+](=O)[O-])[N+](=O)[O-])N(C(=O)N2[N+](=O)[O-])[N+](=O)[O-]

Technology Process of Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro-

There total 5 articles about Imidazo[4,5-d]imidazole-2,5(1H,3H)-dione, tetrahydro-1,3,4,6-tetranitro- 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: 85.0%

glycoluril (496-46-8) → 2,4,6,8-tetranitro-2,4,6,8-tetraazabicyclo<3.3.0>octane-3,7-dione (55510-03-7)

Guidance literature:

With nitric acid; dinitrogen pentoxide;

Reference yield: 80.0%

octahydro-5-imino-2-nitroiminoimidazo<4,5-d>imidazole mononitrate salt → 2,4,6,8-tetranitro-2,4,6,8-tetraazabicyclo<3.3.0>octane-3,7-dione (55510-03-7)

Guidance literature:

With nitric acid; trifluoroacetic anhydride; calcium chloride; at 0 - 20 ℃; for 2h; Inert atmosphere;

Reference yield: 75.0%

mononitroglycoluril (97095-19-7) → 2,4,6,8-tetranitro-2,4,6,8-tetraazabicyclo<3.3.0>octane-3,7-dione (55510-03-7)

Guidance literature:

With nitric acid; dinitrogen pentoxide; at 15 ℃; for 2h;

upstream raw materials:

glycoluril

mononitroglycoluril