4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine

Base Information

Chemical Name:4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine
CAS No.:112467-60-4
Molecular Formula:C12H8ClN3O
Molecular Weight:245.668
Hs Code.:
DSSTox Substance ID:DTXSID20551600
Wikidata:Q82431352

Synonyms:112467-60-4;4-Chloro-3-(p-tolyl)isoxazolo[5,4-d]pyrimidine;DTXSID20551600;4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine;AKOS015936664;4-chloro-3-(4-methylphenyl)isoxazolo[5,4-d]pyrimidine

Suppliers and Price of 4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine

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
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price

Total 1 raw suppliers

Chemical Property of 4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:245.0355896
Heavy Atom Count:17
Complexity:271

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C2=NOC3=C2C(=NC=N3)Cl

Technology Process of 4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine

There total 3 articles about 4-Chloro-3-(4-methylphenyl)[1,2]oxazolo[5,4-d]pyrimidine 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: 56.0%

: 117840-05-8
4,5-dihydro-4-oxo-3-(p-tolyl)isoxazolo<5,4-d>pyrimidine

: 112467-60-4
4-chloro-3-(p-tolyl)isoxazolo<5,4-d>pyrimidine

Guidance literature:: With trichlorophosphate; for 2.5h; Heating;

Reference yield:

: 36288-37-6
(Z)-N-hydroxy-4-methylbenzene-1-carbonimidoyl chloride

: 112467-60-4
4-chloro-3-(p-tolyl)isoxazolo<5,4-d>pyrimidine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) EtONa / 1.) EtOH, 2.) EtOH, a) RT, 1.5 h, b) reflux, 2.5 h

2: 77.8 percent / Ac₂O / 3 h / Heating

3: 56 percent / POCl₃ / 2.5 h / Heating

With sodium ethanolate; acetic anhydride; trichlorophosphate;

Reference yield:

: 137145-81-4
5-amino-3-(p-tolyl)isoxazole-4-carboxamide

: 112467-60-4
4-chloro-3-(p-tolyl)isoxazolo<5,4-d>pyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 77.8 percent / Ac₂O / 3 h / Heating

2: 56 percent / POCl₃ / 2.5 h / Heating

With acetic anhydride; trichlorophosphate;