2-Benzyl-3-phenyloxaziridine

Base Information

Chemical Name:2-Benzyl-3-phenyloxaziridine
CAS No.:7731-37-5
Molecular Formula:C14H13NO
Molecular Weight:211.263
Hs Code.:
Mol file:7731-37-5.mol

Synonyms:2-Benzyl-3-phenyl-chinolin-4-ol;2-benzyl-3-phenyl oxaziridine;4-Hydroxy-3-phenyl-2-benzyl-chinolin;2-Benzyl-3-phenyl-oxaziridin;2-benzyl-3-phenyl-quinolin-4-ol;

Suppliers and Price of 2-Benzyl-3-phenyloxaziridine

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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Total 0 raw suppliers

Chemical Property of 2-Benzyl-3-phenyloxaziridine

Chemical Property:

Boiling Point:321℃
Flash Point:98℃
PSA：15.54000
Density:1.187
LogP:3.07050

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Benzyl-3-phenyloxaziridine

There total 5 articles about 2-Benzyl-3-phenyloxaziridine 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: 95.0%

: 780-25-6
N-benzylidene benzylamine

: 7731-37-5
2-benzyl-3-phenyl-1,2-oxaziridine

Guidance literature:: With maleic anhydride; urea hydrogen peroxide adduct; In methanol; at 0 ℃; for 0.666667h;
DOI:10.1055/s-2002-31903

Reference yield:

: 3376-26-9
N-Benzylidenebenzylamine N-oxide

: 7731-37-5
2-benzyl-3-phenyl-1,2-oxaziridine

Guidance literature:: In [⁽²⁾H₆]acetone; at 20 ℃; for 4h; Inert atmosphere; UV-irradiation;
DOI:10.1039/c5ob01277e

Reference yield:

: 100-52-7
benzaldehyde

: 7731-37-5
2-benzyl-3-phenyl-1,2-oxaziridine

Guidance literature:: Multi-step reaction with 2 steps

1: MgSO₄ / CH₂Cl₂ / 2 h / 20 °C

2: m-chloroperbenzoic acid / CH₂Cl₂ / 4 h / 4 °C

With magnesium sulfate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1016/S0968-0896(01)00003-7