4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-

Base Information

Chemical Name:4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-
CAS No.:52169-85-4
Molecular Formula:C₁₃H₁₃FN₂O₂
Molecular Weight:248.257
Hs Code.:
DSSTox Substance ID:DTXSID20484080
Wikidata:Q82322092
Mol file:52169-85-4.mol

Synonyms:52169-85-4;N-Ethyl-2-(2-fluorophenyl)-5-methyloxazole-4-carboxamide;4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-;SCHEMBL11620376;DTXSID20484080

Suppliers and Price of 4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-

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 0 raw suppliers

Chemical Property of 4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:248.09610582
Heavy Atom Count:18
Complexity:301

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCNC(=O)C1=C(OC(=N1)C2=CC=CC=C2F)C

Technology Process of 4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-methyl-

There total 5 articles about 4-Oxazolecarboxamide, N-ethyl-2-(2-fluorophenyl)-5-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:

: 61151-91-5
2-(4-chloro-benzoylamino)-3-oxo-butyric acid ethyl ester

: 52169-85-4
2-(2-fluoro-phenyl)-5-methyl-oxazole-4-carboxylic acid ethylamide

Guidance literature:: Multi-step reaction with 4 steps

1: POCl₃ / benzene / Heating

2: NaOH / ethanol

3: SOCl₂ / dimethylformamide

With sodium hydroxide; thionyl chloride; trichlorophosphate; In ethanol; N,N-dimethyl-formamide; benzene;

Reference yield:

: 122-01-0
4-chloro-benzoyl chloride

: 52169-85-4
2-(2-fluoro-phenyl)-5-methyl-oxazole-4-carboxylic acid ethylamide

Guidance literature:: Multi-step reaction with 5 steps

1: (i) Zn, aq. H₂SO₄, (ii) /BRN= 471606/

2: POCl₃ / benzene / Heating

3: NaOH / ethanol

4: SOCl₂ / dimethylformamide

With sodium hydroxide; thionyl chloride; trichlorophosphate; In ethanol; N,N-dimethyl-formamide; benzene;

Reference yield:

: 61151-98-2
2-(2-fluoro-phenyl)-5-methyl-oxazole-4-carboxylic acid ethyl ester

: 52169-85-4
2-(2-fluoro-phenyl)-5-methyl-oxazole-4-carboxylic acid ethylamide

Guidance literature:: Multi-step reaction with 3 steps

1: NaOH / ethanol

2: SOCl₂ / dimethylformamide

With sodium hydroxide; thionyl chloride; In ethanol; N,N-dimethyl-formamide;