5-Chloro-4-methyl-3-phenyl-1,2-oxazole

Base Information

Chemical Name:5-Chloro-4-methyl-3-phenyl-1,2-oxazole
CAS No.:3356-90-9
Molecular Formula:C10H8ClNO
Molecular Weight:193.633
Hs Code.:
DSSTox Substance ID:DTXSID20542114
Wikidata:Q82418652

Synonyms:3356-90-9;5-chloro-4-methyl-3-phenylisoxazole;5-Chloro-4-methyl-3-phenyl-1,2-oxazole;DTXSID20542114

Suppliers and Price of 5-Chloro-4-methyl-3-phenyl-1,2-oxazole

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 1 raw suppliers

Chemical Property of 5-Chloro-4-methyl-3-phenyl-1,2-oxazole

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:193.0294416
Heavy Atom Count:13
Complexity:170

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(ON=C1C2=CC=CC=C2)Cl

Technology Process of 5-Chloro-4-methyl-3-phenyl-1,2-oxazole

There total 4 articles about 5-Chloro-4-methyl-3-phenyl-1,2-oxazole 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: 100.0%

: 23244-37-3
4-methyl-3-phenylisoxazole-5(4H)-one

: 3356-90-9
5-chloro-4-methyl-3-phenylisoxazole

Guidance literature:: With triethylamine; trichlorophosphate; at 104 ℃; for 13h;
DOI:10.1002/anie.202004243

Reference yield:

: 94-02-0
ethyl 3-oxo-3-phenylpropionate

: 3356-90-9
5-chloro-4-methyl-3-phenylisoxazole

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 2 h / Reflux

2: hydroxylamine hydrochloride; pyridine / ethanol / 2 h / Reflux

3: trichlorophosphate; triethylamine / 13 h / Reflux

With pyridine; hydroxylamine hydrochloride; potassium carbonate; triethylamine; trichlorophosphate; In ethanol; acetone;
DOI:10.1002/anie.201710920

Reference yield:

: 10488-87-6
ethyl 2-benzoylpropionate

: 3356-90-9
5-chloro-4-methyl-3-phenylisoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride; pyridine / ethanol / 2 h / Reflux

2: trichlorophosphate; triethylamine / 13 h / Reflux

With pyridine; hydroxylamine hydrochloride; triethylamine; trichlorophosphate; In ethanol;
DOI:10.1002/anie.201710920