3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide

Base Information

Chemical Name:3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide
CAS No.:99052-48-9
Molecular Formula:C19H22N2O2
Molecular Weight:310.3902
Hs Code.:
DSSTox Substance ID:DTXSID50912886

Synonyms:3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide;4-(2,5-Dihydro-2,2-dimethyl-4-phenyl-5-oxazolyl)-N,N-dimethylbenzenamine N-oxide;5-(p-(Dimethyl-oxido-ammonio)phenyl)-2,2-dimethyl-4-phenyl-delta(sup 3)-1,3-oxazolin [German];Benzenamine, 4-(2,5-dihydro-2,2-dimethyl-4-phenyl-5-oxazolyl)-N,N-dimethyl-, N-oxide;99052-48-9;5-(p-(Dimethyl-oxido-ammonio)phenyl)-2,2-dimethyl-4-phenyl-delta(sup 3)-1,3-oxazolin;DTXSID50912886;LS-28268;4-(2,2-Dimethyl-4-phenyl-2,5-dihydro-1,3-oxazol-5-yl)-N,N-dimethylbenzen-1-amine N-oxide

Suppliers and Price of 3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide

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 3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:310.168127949
Heavy Atom Count:23
Complexity:444

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(N=C(C(O1)C2=CC=C(C=C2)[N+](C)(C)[O-])C3=CC=CC=C3)C

Technology Process of 3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide

There total 3 articles about 3-Oxazoline, 2,2-dimethyl-5-(p-(dimethylamino)phenyl)-4-phenyl-, N-oxide 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: 68.6%

: 79213-82-4
5--2,2-dimethyl-4-phenyl-Δ³-1,3-oxazolin

: 99052-48-9
5--2,2-dimethyl-4-phenyl-Δ³-1,3-oxazolin

Guidance literature:: With dihydrogen peroxide; In acetic anhydride; for 2.5h;
DOI:10.1002/hlca.19850680308

Reference yield:

: 100-10-7
4-dimethylamino-benzaldehyde

: 99052-48-9
5--2,2-dimethyl-4-phenyl-Δ³-1,3-oxazolin

Guidance literature:: Multi-step reaction with 2 steps

1: 59.6 percent / dioxane / 1.5 h / Irradiation

2: 68.6 percent / 30 percent H₂O₂ / acetic anhydride / 2.5 h

With dihydrogen peroxide; In 1,4-dioxane; acetic anhydride;
DOI:10.1002/hlca.19850680308

Reference yield:

: 14491-02-2
2,2-dimethyl-3-phenyl-2H-azirine

: 99052-48-9
5--2,2-dimethyl-4-phenyl-Δ³-1,3-oxazolin

Guidance literature:: Multi-step reaction with 2 steps

1: 59.6 percent / dioxane / 1.5 h / Irradiation

2: 68.6 percent / 30 percent H₂O₂ / acetic anhydride / 2.5 h

With dihydrogen peroxide; In 1,4-dioxane; acetic anhydride;
DOI:10.1002/hlca.19850680308