2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid

Base Information

Chemical Name:2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid
CAS No.:131467-94-2
Molecular Formula:C₁₀H₈N₂O₃
Molecular Weight:204.185
Hs Code.:
DSSTox Substance ID:DTXSID801280576

Synonyms:2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid;131467-94-2;2-(5-Phenyl-1,3,4-oxadiazol-2-yl)aceticacid;DTXSID801280576;MFCD03414708;AKOS004117884;NS-02133;5-Phenyl-1,3,4-oxadiazole-2-acetic acid;EN300-251849;Z1508933471

Suppliers and Price of 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:204.05349212
Heavy Atom Count:15
Complexity:229

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN=C(O2)CC(=O)O

Technology Process of 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid

There total 5 articles about 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetic Acid 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: 80.0%

: 4882-92-2
ethyl 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetate

: 131467-94-2
(5-phenyl-[1,3,4]oxadiazol-2-yl)acetic acid

Guidance literature:: ethyl 2-(5-phenyl-1,3,4-oxadiazol-2-yl)acetate; With potassium hydroxide; In ethanol; at 20 ℃; for 3h;

With hydrogenchloride; In water;
DOI:10.1515/HC.2001.7.5.411

Reference yield:

: 98-88-4
benzoyl chloride

: 131467-94-2
(5-phenyl-[1,3,4]oxadiazol-2-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 44 percent / pyridine / 0.75 h / Heating

2.1: potassium hydroxide / ethanol / 3 h / 20 °C

2.2: 80 percent / hydrochloric acid / H₂O

With potassium hydroxide; In pyridine; ethanol;
DOI:10.1515/HC.2001.7.5.411

Reference yield:

: 4874-92-4
2'-benzoyl-2-ethoxycarbonylacetohydrazide

: 131467-94-2
(5-phenyl-[1,3,4]oxadiazol-2-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 3 h / Heating

2: lithium hydroxide / water; methanol; tetrahydrofuran / 5 h / 20 °C

With lithium hydroxide; trichlorophosphate; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.ejmech.2019.111867