Piperazine, 1-(6-hexyl-2-pyridinyl)-

Base Information

Chemical Name:Piperazine, 1-(6-hexyl-2-pyridinyl)-
CAS No.:120144-99-2
Molecular Formula:C₁₅H₂₅N₃
Molecular Weight:247.384
Hs Code.:
DSSTox Substance ID:DTXSID30152703
Wikidata:Q83019415
ChEMBL ID:CHEMBL21495

Synonyms:BRN 6510465;Piperazine, 1-(6-hexyl-2-pyridinyl)-;1-(6-Hexyl-2-pyridinyl)piperazine;120144-99-2;CHEMBL21495;DTXSID30152703;LS-112705

Suppliers and Price of Piperazine, 1-(6-hexyl-2-pyridinyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Piperazine, 1-(6-hexyl-2-pyridinyl)-

Chemical Property:

Vapor Pressure:1.68E-06mmHg at 25°C
Boiling Point:396.7°Cat760mmHg
Flash Point:193.7°C
Density:0.99g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:247.204847810
Heavy Atom Count:18
Complexity:214

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC1=NC(=CC=C1)N2CCNCC2

Technology Process of Piperazine, 1-(6-hexyl-2-pyridinyl)-

There total 2 articles about Piperazine, 1-(6-hexyl-2-pyridinyl)- 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: 63.0%

: 110-85-0
piperazine

: 109201-48-1
2-chloro-6-hexylpyridine

: 120144-99-2
1-(6-hexyl-2-pyridinyl)piperazine

Guidance literature:: In butan-1-ol; for 48h; Heating;
DOI:10.1021/jm00126a015

Reference yield:

: 111-13-7
hexyl-methyl-ketone

: 120144-99-2
1-(6-hexyl-2-pyridinyl)piperazine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 g / Na / diethyl ether

2: 63 percent / butan-1-ol / 48 h / Heating

With sodium; In diethyl ether; butan-1-ol;
DOI:10.1021/jm00126a015