Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-

Base Information

Chemical Name:Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-
CAS No.:151392-12-0
Molecular Formula:C₁₇H₁₆N₄O₃
Molecular Weight:324.339
Hs Code.:
DSSTox Substance ID:DTXSID30164780
Nikkaji Number:J578.288K
Wikidata:Q83033856
Mol file:151392-12-0.mol

Synonyms:N-(4-((5-(Phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)acetamide;Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-;151392-12-0;N-[4-[[5-(Phenylamino)-1,3,4-oxadiazol-2-yl]methoxy]phenyl]acetamide;DTXSID30164780

Suppliers and Price of Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-

Supply Marketing:

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

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Chemical Property of Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-

Chemical Property:

PSA：96.00000
Density:1.337g/cm³
LogP:3.42200
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:324.12224039
Heavy Atom Count:24
Complexity:395

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)OCC2=NN=C(O2)NC3=CC=CC=C3

Technology Process of Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)-

There total 4 articles about Acetamide, N-(4-((5-(phenylamino)-1,3,4-oxadiazol-2-yl)methoxy)phenyl)- 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: 64.8%

: 151392-08-4
N¹-<(acetamidophen-4-yl)oxy>acetyl-N⁴-phenyl-3-thiosemicarbazide

: 151392-12-0
5-<(acetamidophen-4-yl)oxy>methyl-2-phenylamino-1,3,4-oxadiazole

Guidance literature:: With sodium hydroxide; iodine; potassium iodide; In ethanol; water; Ambient temperature;
DOI:10.1002/jps.2600830226

Reference yield:

: 67202-81-7
ethyl 2-[4-(acetylamino)phenoxy]acetate

: 151392-12-0
5-<(acetamidophen-4-yl)oxy>methyl-2-phenylamino-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: 67.2 percent / 99percent hydrazine hydrate / ethanol / 2 h / Heating

2: 81.57 percent / ethanol / 4 h / Heating

3: 64.8 percent / 2N NaOH, I₂, 5percent KI / ethanol; H₂O / Ambient temperature

With sodium hydroxide; iodine; hydrazine hydrate; potassium iodide; In ethanol; water;
DOI:10.1002/jps.2600830226

Reference yield:

: 75129-75-8
N‐(4‐(2‐hydrazinyl‐2‐oxoethoxy)phenyl) acetamide

: 151392-12-0
5-<(acetamidophen-4-yl)oxy>methyl-2-phenylamino-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 81.57 percent / ethanol / 4 h / Heating

2: 64.8 percent / 2N NaOH, I₂, 5percent KI / ethanol; H₂O / Ambient temperature

With sodium hydroxide; iodine; potassium iodide; In ethanol; water;
DOI:10.1002/jps.2600830226