1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-

Base Information

Chemical Name:1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-
CAS No.:73484-50-1
Molecular Formula:C₁₆H₁₂ClN₃O₄
Molecular Weight:345.742
Hs Code.:
DSSTox Substance ID:DTXSID00223691
Wikidata:Q83102168

Synonyms:1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-;5-(1,3-Benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-1,3,4-oxadiazol-2(3H)-one;73484-50-1;C16H12ClN3O4;DTXSID00223691;LS-99309

Suppliers and Price of 1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-

Supply Marketing:

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

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Chemical Property of 1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-

Chemical Property:

Vapor Pressure:9E-11mmHg at 25°C
Boiling Point:516.4°Cat760mmHg
Flash Point:266.1°C
Density:1.55g/cm³
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:345.0516336
Heavy Atom Count:24
Complexity:510

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1OC2=C(O1)C=C(C=C2)C3=NN(C(=O)O3)CNC4=CC=C(C=C4)Cl

Technology Process of 1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)methyl)-

There total 1 articles about 1,3,4-Oxadiazol-2(3H)-one, 5-(1,3-benzodioxol-5-yl)-3-(((4-chlorophenyl)amino)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: 95.0%