N-(2,4,6-trinitrophenyl)pyridin-2-amine

Base Information

Chemical Name:N-(2,4,6-trinitrophenyl)pyridin-2-amine
CAS No.:39771-29-4
Molecular Formula:C₁₁H₇N₅O₆
Molecular Weight:305.206
Hs Code.:
European Community (EC) Number:652-088-0
DSSTox Substance ID:DTXSID00389009
Wikidata:Q82184346
ChEMBL ID:CHEMBL1538410
Mol file:39771-29-4.mol

Synonyms:N-(2,4,6-trinitrophenyl)pyridin-2-amine;39771-29-4;MLS000712446;N-(2,4,6-TRINITROPHENYL)-2-PYRIDINAMINE;SMR000282213;2-picrylaminopyridine;picryl(2-pyridyl)amine;CHEMBL1538410;BDBM34896;cid_3089122;DTXSID00389009;REGID_for_CID_3089122;HMS2699H03;STL417074;STL507153;AKOS000416978;AKOS000540684;AKOS016032220;FT-0744699;A824726;SR-01000313653;2,4,6-trinitro-N-(pyridin-2(1H)-ylidene)aniline;SR-01000313653-1;pyridin-2-yl-(2,4,6-trinitro-phenyl)-amine;2-N-(2,4,6-trinitrophenyl)pyridineamine

Suppliers and Price of N-(2,4,6-trinitrophenyl)pyridin-2-amine

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

Sigma-Aldrich
N-(2-PYRIDYL)PICRYLAMINE Aldrich
250mg
$ 144.00

American Custom Chemicals Corporation
N-(2-PYRIDYL)PICRYLAMINE 95.00%
5MG
$ 498.86

Total 5 raw suppliers

Chemical Property of N-(2,4,6-trinitrophenyl)pyridin-2-amine

Chemical Property:

PSA：162.38000
LogP:4.19240
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:2
Exact Mass:305.03963296
Heavy Atom Count:22
Complexity:420

Purity/Quality:

97% ^*data from raw suppliers

N-(2-PYRIDYL)PICRYLAMINE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=NC(=C1)NC2=C(C=C(C=C2[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]

Technology Process of N-(2,4,6-trinitrophenyl)pyridin-2-amine

There total 4 articles about N-(2,4,6-trinitrophenyl)pyridin-2-amine 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: 80.0%