2,3-Dihydroxy-1,4-phenazinedione

Base Information

• Chemical Name: 2,3-Dihydroxy-1,4-phenazinedione
• CAS No.: 23774-13-2
• Molecular Formula: C12H6 N2 O4
• Molecular Weight: 242.187
• Hs Code.: 2933990090
• European Community (EC) Number: 654-136-6
• NSC Number: 111181
• UNII: F5J3YZR5HG
• DSSTox Substance ID: DTXSID60946571
• Nikkaji Number: J50.004F
• Mol file: 23774-13-2.mol

Synonyms:2,3-Dihydroxy-1,4-phenazinedione;23774-13-2;5,10-dihydrophenazine-1,2,3,4-tetrone;1,4-PHENAZINEDIONE, 2,3-DIHYDROXY-;2,3-Dihydroxy-1,4-phenazinequinone;2,3-Dihydroxyphenazine-1,4-quinone;F5J3YZR5HG;NSC 111181;BRN 0237377;NSC-111181;2 3-DIHYDROXY-1 4-PHENAZINEDIONE;2,3-DIHYDROXYPHENAZINE-1,4-DIONE;5-25-03-00374 (Beilstein Handbook Reference);2,4-phenazinedione;NSC111181;2,4-phenazinequinone;UNII-F5J3YZR5HG;SCHEMBL8463317;C12H6N2O4;DTXSID60946571;ADXGUJPMVBJHFH-UHFFFAOYSA-N;C12-H6-N2-O4;AKOS024323374;23-DIHYDROXY-14-PHENAZINEDIONE;LS-103020

Chemical Property of 2,3-Dihydroxy-1,4-phenazinedione

Chemical Property:

• Vapor Pressure: 5.09E-07mmHg at 25°C
• Boiling Point: 412.7°Cat760mmHg
• Flash Point: 180.7°C
• PSA: 100.38000
• Density: 1.64g/cm³
• LogP: 1.33640
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 242.03275668
• Heavy Atom Count: 18
• Complexity: 474

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,3-DIHYDROXY-1,4-PHENAZINEDIONE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)NC3=C(N2)C(=O)C(=O)C(=O)C3=O

Technology Process of 2,3-Dihydroxy-1,4-phenazinedione

There total 3 articles about 2,3-Dihydroxy-1,4-phenazinedione 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:

phenazine-1,2,3,4-tetraone (23774-19-8) → 2.3-Dihydroxy-phenazin-1.4-chinon (23774-13-2)

Guidance literature:

With air;

Reference yield:

rhodizonic acid (118-76-3) + 1,2-diamino-benzene (95-54-5) → 2.3-Dihydroxy-phenazin-1.4-chinon (23774-13-2)

Guidance literature:

With hydrogenchloride;

Reference yield:

→ 2.3-Dihydroxy-phenazin-1.4-chinon (23774-13-2)

Guidance literature:

Rhodizonsaeuredihydrat, o-Phenylendiamin, wss. H2SO4;

DOI:10.1016/S0040-4020(01)82926-4

upstream raw materials:

phenazine-1,2,3,4-tetraone

rhodizonic acid

1,2-diamino-benzene