10H-Phenoxazine-3,7-diamine

Base Information

• Chemical Name: 10H-Phenoxazine-3,7-diamine
• CAS No.: 4935-76-6
• Molecular Formula: C12H11N3O
• Molecular Weight: 213.239
• DSSTox Substance ID: DTXSID80552310
• Nikkaji Number: J1.978.585H
• Wikidata: Q82432477
• Mol file: 4935-76-6.mol

Synonyms:10H-Phenoxazine-3,7-diamine;4935-76-6;SCHEMBL1448832;DTXSID80552310

Chemical Property of 10H-Phenoxazine-3,7-diamine

Chemical Property:

• XLogP3: 2.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 213.090211983
• Heavy Atom Count: 16
• Complexity: 237

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C(C=C1N)OC3=C(N2)C=CC(=C3)N

Technology Process of 10H-Phenoxazine-3,7-diamine

There total 1 articles about 10H-Phenoxazine-3,7-diamine 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:

C12H10N3O → oxonine (53669-98-0) + 10H-phenoxazine-3,7-diamine (4935-76-6)

Guidance literature:

Rate constant; disproportionation, further reaction with Fe(III);

DOI:10.1039/c39810000497

Reference yield:

3-fluoro-1-nitrobenzene (402-67-5) + 10H-phenoxazine-3,7-diamine (4935-76-6) → N3,N7-bis(3-nitrophenyl)-10H-phenoxazine-3,7-diamine

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 150 ℃; for 12h; Inert atmosphere;

Reference yield:

4-fluoro-N-(4-nitrophenyl)aniline (330-89-2) + 10H-phenoxazine-3,7-diamine (4935-76-6) → N1,N1'-(10H-phenoxazine-3,7-diyl)bis(N4-(4-nitrophenyl)benzene-1,4-diamine)

Guidance literature:

With potassium carbonate; In dimethyl sulfoxide; at 150 ℃; for 12h; Inert atmosphere;

Downstream raw materials:

oxonine