2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole

Base Information

Chemical Name:2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole
CAS No.:402939-29-1
Molecular Formula:C15H9Cl3N2O2
Molecular Weight:355.608
Hs Code.:
DSSTox Substance ID:DTXSID001185259

Synonyms:DTXSID001185259;2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole;402939-29-1

Suppliers and Price of 2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole

Supply Marketing:

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

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Chemical Property of 2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:353.972961
Heavy Atom Count:22
Complexity:346

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN=C(O2)COC3=C(C=C(C=C3Cl)Cl)Cl

Technology Process of 2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole

There total 4 articles about 2-Phenyl-5-[(2,4,6-trichlorophenoxy)methyl]-1,3,4-oxadiazole 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: 92.0%

: 65-85-0,8013-63-6
benzoic acid

: 190588-40-0
2-(2,4,6-trichlorophenoxy)acetic acid hydrazide

: 402939-29-1
2-phenyl-5-(2,4,6-trichloro-phenoxymethyl)-[1,3,4]oxadiazole

Guidance literature:: In trichlorophosphate; at 110 - 120 ℃; for 15h;

Reference yield:

: 14426-43-8
ethyl 2-(2,4,6-trichlorophenoxy)acetate

: 402939-29-1
2-phenyl-5-(2,4,6-trichloro-phenoxymethyl)-[1,3,4]oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / hydrazine hydrate / ethanol / 5 h / Heating

2: POCl₃ / Heating

With hydrazine hydrate; trichlorophosphate; In ethanol;

Reference yield:

: 88-06-2,67471-29-8
2,4,6-Trichlorophenol

: 402939-29-1
2-phenyl-5-(2,4,6-trichloro-phenoxymethyl)-[1,3,4]oxadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / K₂CO₃ / acetone / 6 h / Heating

2: 74 percent / hydrazine hydrate / ethanol / 5 h / Heating

3: POCl₃ / Heating

With potassium carbonate; hydrazine hydrate; trichlorophosphate; In ethanol; acetone;