2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride

Base Information

Chemical Name:2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride
CAS No.:127718-43-8
Molecular Formula:C25H24 Cl N6 O2 . Cl
Molecular Weight:511.4031
Hs Code.:
Mol file:127718-43-8.mol

Synonyms:127718-43-8;2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride;LS-149208

Suppliers and Price of 2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride

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
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Total 1 raw suppliers

Chemical Property of 2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:510.1337794
Heavy Atom Count:35
Complexity:664

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCN1CC(=O)N2N=C(N=[N+]2C3=CC=C(C=C3)Cl)C4=CC=CC=C4O)C5=CC=CC=C5.[Cl-]

Technology Process of 2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride

There total 5 articles about 2H-Tetrazolium, 3-(4-chlorophenyl)-5-(2-hydroxyphenyl)-2-((4-phenyl-1-piperazinyl)acetyl)-, chloride 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: 60.0%

: 127718-39-2
(4-Phenyl-piperazin-1-yl)-acetic acid [1-(4-chloro-phenylazo)-1-(2-hydroxy-phenyl)-meth-(E)-ylidene]-hydrazide

: 127718-43-8
2-(4-Chloro-phenyl)-5-(2-hydroxy-phenyl)-3-[2-(4-phenyl-piperazin-1-yl)-acetyl]-3H-tetrazol-2-ium; chloride

Guidance literature:: With sulfuric acid; dihydrogen peroxide; iron(II) sulfate; In ethanol; at 100 ℃; for 3h;

Reference yield:

: 127718-30-3
4-phenyl-1-piperazineacetic acid salicylidenehydrazide

: 127718-43-8
2-(4-Chloro-phenyl)-5-(2-hydroxy-phenyl)-3-[2-(4-phenyl-piperazin-1-yl)-acetyl]-3H-tetrazol-2-ium; chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) sodium nitrite, HCl / 1.) gl. acetic acid, 0-5 deg C, 2.) pyridine, RT, overnight

2: 60 percent / 20percent H₂O₂, FeSO₄, H₂SO₄ / ethanol / 3 h / 100 °C

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

Reference yield:

: 106-47-8
4-chloro-aniline

: 127718-43-8
2-(4-Chloro-phenyl)-5-(2-hydroxy-phenyl)-3-[2-(4-phenyl-piperazin-1-yl)-acetyl]-3H-tetrazol-2-ium; chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) sodium nitrite, HCl / 1.) gl. acetic acid, 0-5 deg C, 2.) pyridine, RT, overnight

2: 60 percent / 20percent H₂O₂, FeSO₄, H₂SO₄ / ethanol / 3 h / 100 °C

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