2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-oxazole

Base Information

Chemical Name:2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-oxazole
CAS No.:105359-79-3
Molecular Formula:C13H17NO
Molecular Weight:203.284
Hs Code.:
DSSTox Substance ID:DTXSID50550808
Nikkaji Number:J1.730.352J
Wikidata:Q82430266
Mol file:105359-79-3.mol

Synonyms:105359-79-3;2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-oxazole;SCHEMBL1660986;DTXSID50550808

Suppliers and Price of 2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-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 0 raw suppliers

Chemical Property of 2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-oxazole

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:203.131014166
Heavy Atom Count:15
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)C2=NCCO2

Technology Process of 2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-oxazole

There total 5 articles about 2-(4-tert-Butylphenyl)-4,5-dihydro-1,3-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: 88.0%

: 877-65-6
p-tert-butylbenzyl alcohol

: 141-43-5
ethanolamine

: 105359-79-3
2-(4-(tert-butyl)phenyl)-4,5-dihydrooxazole

Guidance literature:: p-tert-butylbenzyl alcohol; With iodine; potassium carbonate; In tert-butyl alcohol; at 70 ℃; for 8h;

ethanolamine; In tert-butyl alcohol; at 70 ℃; for 18h;
DOI:10.1016/j.tet.2006.11.077