4-Oxazolecarboxamide, 5-methyl-2-phenyl-

Base Information

Chemical Name:4-Oxazolecarboxamide, 5-methyl-2-phenyl-
CAS No.:51655-72-2
Molecular Formula:C11H10N2O2
Molecular Weight:202.21
Hs Code.:
NSC Number:290944
UNII:CT3LD1G0TG
DSSTox Substance ID:DTXSID90199593
Nikkaji Number:J78.627F
Wikidata:Q83072498
Mol file:51655-72-2.mol

Synonyms:4-Oxazolecarboxamide, 5-methyl-2-phenyl-;51655-72-2;5-Methyl-2-phenyloxazole-4-carboxamide;5-methyl-2-phenyl-1,3-oxazole-4-carboxamide;Oxazole-4-carboxamide, 5-methyl-2-phenyl-;CT3LD1G0TG;NSC 290944;5-methyl-2-phenyl-4-oxazolecarboxamide;BRN 0911987;Oxazole-4-carboxamide, 5-methyl-2-phenyl- ethyl)-, monohydrochloride;NSC-290944;NSC290944;UNII-CT3LD1G0TG;SCHEMBL167906;DTXSID90199593;4-Carbamoyl-5-methyl-2-phenyloxazole;LS-100087;A829246

Suppliers and Price of 4-Oxazolecarboxamide, 5-methyl-2-phenyl-

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

American Custom Chemicals Corporation
5-METHYL-2-PHENYLOXAZOLE-4-CARBOXAMIDE 95.00%
5MG
$ 495.40

Total 4 raw suppliers

Chemical Property of 4-Oxazolecarboxamide, 5-methyl-2-phenyl-

Chemical Property:

Vapor Pressure:2.38E-06mmHg at 25°C
Boiling Point:391.9°C at 760 mmHg
Flash Point:190.8°C
PSA：69.12000
Density:1.22g/cm³
LogP:2.44920
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:202.074227566
Heavy Atom Count:15
Complexity:239

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

5-METHYL-2-PHENYLOXAZOLE-4-CARBOXAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=C(O1)C2=CC=CC=C2)C(=O)N

Technology Process of 4-Oxazolecarboxamide, 5-methyl-2-phenyl-

There total 6 articles about 4-Oxazolecarboxamide, 5-methyl-2-phenyl- 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:

: 51655-71-1
2-phenyl-5-methyl-4-oxazolecarboxylic acid chloride

: 51655-72-2
5-methyl-2-phenyl-oxazole-4-carboxylic acid amide

Guidance literature:: With ammonia;

Reference yield:

: 18735-74-5
5-methyl-2-phenyloxazole-4-carboxylic acid

: 51655-72-2
5-methyl-2-phenyl-oxazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / dimethylformamide

2: NH₃

With thionyl chloride; ammonia; In N,N-dimethyl-formamide;

Reference yield:

: 61151-96-0
ethyl 5-methyl-2-phenyloxazole-4-carboxylate

: 51655-72-2
5-methyl-2-phenyl-oxazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: NaOH / ethanol

2: SOCl₂ / dimethylformamide

3: NH₃

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