Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-

Base Information

Chemical Name:Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-
CAS No.:127718-45-0
Molecular Formula:C19H20 N4 O
Molecular Weight:320.3883
Hs Code.:
DSSTox Substance ID:DTXSID10155636
Wikidata:Q83023586
ChEMBL ID:CHEMBL1521346

Synonyms:127718-45-0;Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-;BRN 4202628;1-Phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)piperazine;1-phenyl-4-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]piperazine;MLS000686669;F1749-0027;CHEMBL1521346;DTXSID10155636;HMS1844H04;HMS2242I14;2-phenyl-5-((4-phenylpiperazin-1-yl)methyl)-1,3,4-oxadiazole;CCG-68617;STK737825;AKOS001271008;NCGC00115364-01;SMR000339762;LS-113114;SR-01000151172;SR-01000151172-1;D079-0044;Z46173343;2-phenyl-5-[(4-phenylpiperazino)methyl]-1,3,4-oxadiazole

Suppliers and Price of Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-

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

Total 2 raw suppliers

Chemical Property of Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-

Chemical Property:

Vapor Pressure:6.57E-10mmHg at 25°C
Boiling Point:494.2°Cat760mmHg
Flash Point:252.7°C
Density:1.206g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:320.16371127
Heavy Atom Count:24
Complexity:374

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCN1CC2=NN=C(O2)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)-

There total 3 articles about Piperazine, 1-phenyl-4-((5-phenyl-1,3,4-oxadiazol-2-yl)methyl)- 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: 75.0%

: 67041-03-6
4-phenyl-1-piperazineacetic acid benzylidenehydrazide

: 127718-45-0
1-Phenyl-4-(5-phenyl-[1,3,4]oxadiazol-2-ylmethyl)-piperazine

Guidance literature:: With iron(III) chloride; acetic acid; In water; 1.) 1 h, 2.) RT, 2 d;

Reference yield:

: 100-52-7
benzaldehyde

: 127718-45-0
1-Phenyl-4-(5-phenyl-[1,3,4]oxadiazol-2-ylmethyl)-piperazine

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / acetic acid / ethanol / 5 h / Heating

2: 75 percent / FeCl₃, glacial acetic acid / H₂O / 1.) 1 h, 2.) RT, 2 d

With iron(III) chloride; acetic acid; In ethanol; water;

Reference yield:

: 1689-05-0
4-phenyl-1-piperazineacetic acid hydrazide

: 127718-45-0
1-Phenyl-4-(5-phenyl-[1,3,4]oxadiazol-2-ylmethyl)-piperazine

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / acetic acid / ethanol / 5 h / Heating

2: 75 percent / FeCl₃, glacial acetic acid / H₂O / 1.) 1 h, 2.) RT, 2 d

With iron(III) chloride; acetic acid; In ethanol; water;