2,3,6,7,10,11-hexaaminotriphenylene

Base Information

• Chemical Name: 2,3,6,7,10,11-hexaaminotriphenylene
• CAS No.: 1159202-33-1
• Molecular Formula: C₁₈H₁₈N₆
• Molecular Weight: 318.381
• Mol file: 1159202-33-1.mol

Synonyms:

Chemical Property of 2,3,6,7,10,11-hexaaminotriphenylene

Chemical Property:

• Boiling Point: 795.7±55.0 °C(Predicted)
• PKA: 6.26±0.30(Predicted)
• Density: 1.549±0.06 g/cm3(Predicted)

Purity/Quality:

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

Triphenylene-2,3,6,7,10,11-hexaamine 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Use Description: 2,3,6,7,10,11-hexaaminotriphenylene is a versatile chemical compound with applications across different fields. In materials science, it serves as a key building block for the synthesis of organic and coordination polymers with unique electronic and optical properties. These polymers find use in various advanced technologies, including organic electronic devices like organic light-emitting diodes (OLEDs), field-effect transistors (FETs), and photovoltaic cells, contributing to the development of flexible and efficient electronic components. In the field of chemistry, this compound can act as a ligand in coordination chemistry, forming complexes with metal ions that have applications in catalysis and materials synthesis. Its significance varies depending on the specific research or industrial needs within each field, but overall, it plays a pivotal role in advancing materials science and the development of innovative electronic and optical devices.

Technology Process of 2,3,6,7,10,11-hexaaminotriphenylene

There total 1 articles about 2,3,6,7,10,11-hexaaminotriphenylene 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:

2,3,6,7,10,11-hexaaminotriphenylene hexahydrochloride → triphenylene-2,3,6,7,10,11-hexaamine (1159202-33-1)

Guidance literature:

With triethylamine; In quinoline; at 20 ℃; for 0.5h; Inert atmosphere;

DOI:10.1021/ol202814y

Reference yield:

triphenylene-2,3,6,7,10,11-hexaamine (1159202-33-1) + C16H20N4Ni2O4 → 3C18H18N6*2C6H6N4(4-)*4Ni(2+)

Guidance literature:

In dimethyl sulfoxide; Heating;