2,6-Bis(1H-2-imidazolyl)pyridine

Base Information

Chemical Name:2,6-Bis(1H-2-imidazolyl)pyridine
CAS No.:151674-75-8
Molecular Formula:C₁₁H₉N₅
Molecular Weight:211.226
Hs Code.:2933990090
DSSTox Substance ID:DTXSID80477716
Nikkaji Number:J1.057.521D
Wikidata:Q82310579
Mol file:151674-75-8.mol

Synonyms:151674-75-8;2,6-Bis(1H-2-imidazolyl)pyridine;2,6-Bis-(1H-imidazol-2-yl)-pyridine;2,6-BIS(1H-IMIDAZOL-2-YL)PYRIDINE;Pyridine, 2,6-di-1H-imidazol-2-yl-;2,6-di(1H-imidazol-2-yl)pyridine;2,6-bis(imidazolyl)pyridine;SCHEMBL197279;DTXSID80477716;MFCD08668015

Suppliers and Price of 2,6-Bis(1H-2-imidazolyl)pyridine

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

Crysdot
2,6-Bis(1H-2-imidazolyl)pyridine 95+%
1g
$ 775.00

Chemenu
2,6-Bis(1H-2-imidazolyl)pyridine 95%
1g
$ 732.00

American Custom Chemicals Corporation
2,6-BIS-(1H-IMIDAZOL-2-YL)-PYRIDINE 95.00%
1G
$ 1061.16

AccelPharmtech
2,6-di-1H-imidazol-2-yl-Pyridine 97.00%
25G
$ 3120.00

AccelPharmtech
2,6-di-1H-imidazol-2-yl-Pyridine 97.00%
1G
$ 1530.00

Total 8 raw suppliers

Chemical Property of 2,6-Bis(1H-2-imidazolyl)pyridine

Chemical Property:

PSA：70.25000
LogP:1.86180
XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:211.08579531
Heavy Atom Count:16
Complexity:212

Purity/Quality:

98% ^*data from raw suppliers

2,6-Bis(1H-2-imidazolyl)pyridine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=NC(=C1)C2=NC=CN2)C3=NC=CN3

Technology Process of 2,6-Bis(1H-2-imidazolyl)pyridine

There total 5 articles about 2,6-Bis(1H-2-imidazolyl)pyridine 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%

: 2,6-bis(N-ethoxymethylimidazol-2-yl)pyridine

: 151674-75-8
2,6-bis(1H-imidazole-2-yl)pyridine

Guidance literature:: With hydrogenchloride; In ethanol; Heating;
DOI:10.1039/b313440g

Reference yield:

: 55309-58-5
pyridine-2,6-dicarboximidic acid dimethyl ester

: 645-36-3
2,2-diethoxy-ethanamine

: 151674-75-8
2,6-bis(1H-imidazole-2-yl)pyridine

Guidance literature:: pyridine-2,6-dicarboximidic acid dimethyl ester; 2,2-diethoxy-ethanamine; With acetic acid; In methanol; at 50 ℃; for 1h;

With hydrogenchloride; In methanol; water; for 5h; Reflux;
DOI:10.1016/j.ica.2017.06.073

Reference yield:

: 626-05-1
2,6-Dibromopyridine

: 151674-75-8
2,6-bis(1H-imidazole-2-yl)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 0.25 h / -70 °C

1.2: ZnCl₂ / tetrahydrofuran; hexane / -70 - 20 °C

1.3: 63 percent / Pd(PPh₃)4 / tetrahydrofuran; hexane / Heating

2.1: 80 percent / concn. HCl / ethanol / Heating

With hydrogenchloride; n-butyllithium; In tetrahydrofuran; ethanol; hexane;
DOI:10.1039/b313440g