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2,6,14-triaminotriptycene

Base Information
  • Chemical Name:2,6,14-triaminotriptycene
  • CAS No.:58519-06-5
  • Molecular Formula:C20H17N3
  • Molecular Weight:299.375
  • Hs Code.:
2,6,14-triaminotriptycene

Synonyms:2,6,14-triaminotriptycene

Suppliers and Price of 2,6,14-triaminotriptycene
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
  • Packaging
  • price
  • ChemScene
  • 9,10-Dihydro-9,10-[1,2]benzenoanthracene-2,6,14-triamine
  • 1g
  • $ 1010.00
Total 16 raw suppliers
Chemical Property of 2,6,14-triaminotriptycene
Chemical Property:
  • Melting Point:279-283 °C (decomp) 
  • Boiling Point:534.7±50.0 °C(Predicted) 
  • PKA:5.20±0.20(Predicted) 
  • PSA:78.06000 
  • Density:1.365±0.06 g/cm3(Predicted) 
  • LogP:5.16400 
Purity/Quality:

97% *data from raw suppliers

9,10-Dihydro-9,10-[1,2]benzenoanthracene-2,6,14-triamine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description 2,6,14-Triaminotriptycene is a trisubstituted triptycene derivative with three amino functional groups, serving as a versatile building block for constructing rigid, three-dimensional molecular architectures such as porphyrin arrays, Schiff base sensors, and shape-persistent dendrimers or macrocycles. It is synthesized through controlled nitration and reduction of triptycene, enabling further functionalization for applications in molecular recognition, gas separation membranes, and coordination frameworks. Its rigid scaffold and directional substitution pattern make it valuable for designing materials with tailored porosity or selective binding properties.
Technology Process of 2,6,14-triaminotriptycene

There total 4 articles about 2,6,14-triaminotriptycene 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:
Guidance literature:
With hydrazine hydrate; nickel; In tetrahydrofuran; at 60 ℃;
DOI:10.1021/jo061067t
Guidance literature:
Multi-step reaction with 2 steps
1: 64 percent / HNO3 / 24 h / 75 °C
2: 100 percent / NH2NH2*H2O / Raney Ni / tetrahydrofuran / 60 °C
With nitric acid; hydrazine hydrate; nickel; In tetrahydrofuran;
DOI:10.1021/jo061067t
Guidance literature:
triptycene; With nitric acid;
With hydrazine; nickel; In tetrahydrofuran; Further stages.;
DOI:10.1021/jo701297q
upstream raw materials:

2,6,14-trinitrotriptycene

triptycene

Downstream raw materials:

2,6,14-tris(diphenylamino)triptycene

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