3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide

Base Information

Chemical Name:3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide
CAS No.:87582-49-8
Molecular Formula:C21H15 Cl N5 . I
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID401007667
Mol file:87582-49-8.mol

Synonyms:87582-49-8;3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide;2H-Tetrazolium, 3-(4-chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-, iodide;DTXSID401007667;LS-149209;2-(4-Chlorophenyl)-5-(3H-indol-3-ylidene)-3-phenyl-2,5-dihydro-1H-tetrazol-3-ium iodide

Suppliers and Price of 3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide

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

American Custom Chemicals Corporation
2H-TETRAZOLIUM, 3-(4-CHLOROPHENYL)-5-(1H-INDOL-3-YL)-2-PHENYL-, IODIDE 95.00%
5MG
$ 503.38

Total 3 raw suppliers

Chemical Property of 3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide

Chemical Property:

PSA：49.85000
LogP:-0.23390
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:499.00607
Heavy Atom Count:28
Complexity:491

Purity/Quality:: 2H-TETRAZOLIUM, 3-(4-CHLOROPHENYL)-5-(1H-INDOL-3-YL)-2-PHENYL-, IODIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2N=C(N=[N+]2C3=CC=C(C=C3)Cl)C4=CNC5=CC=CC=C54.[I-]

Technology Process of 3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide

There total 4 articles about 3-(4-Chlorophenyl)-5-(1H-indol-3-yl)-2-phenyl-2H-tetrazolium iodide 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: 40.0%

: 87582-53-4
1-phenyl-3-(3'-indole)-5-(p-chlorophenyl) formazan

: 87582-49-8
2-(4-Chloro-phenyl)-5-(1H-indol-3-yl)-3-phenyl-3H-tetrazol-2-ium; iodide

Guidance literature:: With sulfuric acid; dihydrogen peroxide; iron(II) sulfate; In ethanol; at 100 ℃; for 2h;

Reference yield:

: 487-89-8,1228547-52-1
Indole-3-carboxaldehyde

: 87582-49-8
2-(4-Chloro-phenyl)-5-(1H-indol-3-yl)-3-phenyl-3H-tetrazol-2-ium; iodide

Guidance literature:: Multi-step reaction with 3 steps

1: glacial AcOH / ethanol / 4 h / Heating

2: 1.) conc.HCl, NaNO₂ / 1.) glacial AcOH, H₂O, 0 - 5 deg C, 2.) pyridine, below 10 deg C - room temp.

3: 40 percent / 2 N H₂SO₄, 20percent H₂O₂, FeSO₄ / ethanol / 2 h / 100 °C

With hydrogenchloride; sulfuric acid; dihydrogen peroxide; iron(II) sulfate; acetic acid; sodium nitrite; In ethanol;

Reference yield:

: 16578-92-0
3-[(E)-(2-phenylhydrazinylidene) methyl]-1H-indole

: 87582-49-8
2-(4-Chloro-phenyl)-5-(1H-indol-3-yl)-3-phenyl-3H-tetrazol-2-ium; iodide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) conc.HCl, NaNO₂ / 1.) glacial AcOH, H₂O, 0 - 5 deg C, 2.) pyridine, below 10 deg C - room temp.

2: 40 percent / 2 N H₂SO₄, 20percent H₂O₂, FeSO₄ / ethanol / 2 h / 100 °C

With hydrogenchloride; sulfuric acid; dihydrogen peroxide; iron(II) sulfate; sodium nitrite; In ethanol;