2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine

Base Information

Chemical Name:2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine
CAS No.:63160-14-5
Molecular Formula:C₁₃H₁₀ClNO₃S
Molecular Weight:295.746
Hs Code.:
DSSTox Substance ID:DTXSID001240542

Synonyms:2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine;63160-14-5;DTXSID001240542

Suppliers and Price of 2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:295.0069920
Heavy Atom Count:19
Complexity:408

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2N(O2)S(=O)(=O)C3=CC=C(C=C3)Cl

Technology Process of 2-[(4-Chlorophenyl)sulfonyl]-3-phenyloxaziridine

There total 6 articles about 2-[(4-Chlorophenyl)sulfonyl]-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: 66.0%

: 13707-45-4
N-benzylidene-4-chlorobenzenesulfonamide

: 63160-14-5,64705-28-8,73844-96-9
2-((4-chlorophenyl)sulfonyl)-3-phenyl-1,2-oxaziridine

Guidance literature:: With Oxone; potassium carbonate; In water; toluene; Inert atmosphere;
DOI:10.1021/acs.orglett.6b02417

Reference yield: 45.0%

: 13707-45-4
N-benzylidene-4-chlorobenzenesulfonamide

: 63160-14-5,64705-28-8,73844-96-9
(2S,3S)-2-(4-Chloro-benzenesulfonyl)-3-phenyl-oxaziridine

Guidance literature:: With sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In chloroform; water; for 4h; m-chloroperbenzoic acid was added at 0 deg C over 45 min;
DOI:10.1021/ja00526a040

Reference yield:

: 98-64-6
4-Chlorobenzenesulfonamide

: 63160-14-5,64705-28-8,73844-96-9
(2S,3S)-2-(4-Chloro-benzenesulfonyl)-3-phenyl-oxaziridine

Guidance literature:: Multi-step reaction with 2 steps

1: 0.5 h / 150 - 180 °C

2: 45 percent / NaHCO₃, m-chloroperbenzoic acid / CHCl₃; H₂O / 4 h / m-chloroperbenzoic acid was added at 0 deg C over 45 min

With sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In chloroform; water;
DOI:10.1021/ja00526a040