1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-

Base Information

Chemical Name:1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-
CAS No.:54014-11-8
Molecular Formula:C9H6Cl2N2O2
Molecular Weight:245.0621
Hs Code.:
DSSTox Substance ID:DTXSID00202340
Wikidata:Q83075612
Mol file:54014-11-8.mol

Synonyms:5-(3,4-Dichlorophenyl)-1,3,4-oxadiazole-2-methanol;1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-;54014-11-8;SCHEMBL21792052;DTXSID00202340;LS-99133

Suppliers and Price of 1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-

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 1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-

Chemical Property:

Vapor Pressure:2.14E-07mmHg at 25°C
Boiling Point:408.2°C at 760 mmHg
Flash Point:200.7°C
Density:1.515g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:243.9806328
Heavy Atom Count:15
Complexity:220

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1C2=NN=C(O2)CO)Cl)Cl

Technology Process of 1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)-

There total 4 articles about 1,3,4-Oxadiazole-2-methanol, 5-(3,4-dichlorophenyl)- 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:

: C₁₁H₈Cl₂N₂O₃

: 54014-11-8
[5-(3,4-dichlorophenyl)-1,3,4-oxadiazol-2-yl]methanol

Guidance literature:: With water; potassium carbonate; In methanol; at 20 ℃; for 2h;

Reference yield:

: 33575-81-4
2-(chloromethyl)-5-(3,4-dichlorophenyl)-1,3,4-oxadiazole

: 54014-11-8
[5-(3,4-dichlorophenyl)-1,3,4-oxadiazol-2-yl]methanol

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 18 h / 80 °C

2: potassium carbonate; water / methanol / 2 h / 20 °C

With water; potassium carbonate; In methanol; acetonitrile;

Reference yield:

: 28036-91-1
3,4-dichlorobenzohydrazide

: 54014-11-8
[5-(3,4-dichlorophenyl)-1,3,4-oxadiazol-2-yl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1: trichlorophosphate / Reflux

2: acetonitrile / 18 h / 80 °C

3: potassium carbonate; water / methanol / 2 h / 20 °C

With water; potassium carbonate; trichlorophosphate; In methanol; acetonitrile;