N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea

Base Information

Chemical Name:N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea
CAS No.:89335-11-5
Molecular Formula:C10H10N4O2S
Molecular Weight:250.281
Hs Code.:
DSSTox Substance ID:DTXSID50527292
Wikidata:Q82396456

Synonyms:89335-11-5;N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea;DTXSID50527292

Suppliers and Price of N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea

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 N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:250.05244675
Heavy Atom Count:17
Complexity:271

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2=NN=C(O2)NC(=S)N

Technology Process of N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea

There total 3 articles about N-[5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2-yl]thiourea 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:

: 5711-61-5
2-amino-5-(4-methoxyphenyl)-1,3,4-oxadiazole

: 333-20-0
potassium thioacyanate

: 89335-11-5
N¹-(5-p-methoxyphenyl-1,3,4-oxadiazol-2-yl)thiourea

Guidance literature:: With hydrogenchloride; In ethanol; for 4h; Heating;

Reference yield:

: 6292-71-3,120445-53-6
4-methoxybenzaldehyde semicarbazone

: 89335-11-5
N¹-(5-p-methoxyphenyl-1,3,4-oxadiazol-2-yl)thiourea

Guidance literature:: Multi-step reaction with 2 steps

1: bromine; sodium acetate / acetic acid

2: HCl

With hydrogenchloride; bromine; sodium acetate; In acetic acid;