1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide

Base Information

Chemical Name:1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide
CAS No.:41335-50-6
Molecular Formula:C₁₅H₁₃NO₃S
Molecular Weight:287.339
Hs Code.:
DSSTox Substance ID:DTXSID20961629
Nikkaji Number:J3.569.032H
Mol file:41335-50-6.mol

Synonyms:41335-50-6;1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide;2-(1-Phenylethyl)-1,2-benzisothiazol-3(2H)-one 1,1-dioxide;DTXSID20961629;2-(1-Phenylethyl)-1H-1lambda~6~,2-benzothiazole-1,1,3(2H)-trione

Suppliers and Price of 1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:287.06161445
Heavy Atom Count:20
Complexity:476

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)N2C(=O)C3=CC=CC=C3S2(=O)=O

Technology Process of 1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide

There total 4 articles about 1,2-Benzisothiazol-3(2H)-one, 2-(1-phenylethyl)-, 1,1-dioxide 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: 98.0%

: 99421-72-4
1-phenylethyl 2,2,2-trichloroacetimidate

: 81-07-2
saccharin

: 41335-50-6
3-oxo-N-(1-phenylethyl)benzo[d]isothiazole-2(3h)sulfonamide 1,1-dioxide

Guidance literature:: In toluene; for 18h; Inert atmosphere; Reflux;
DOI:10.1021/acs.joc.6b01421

Reference yield: 92.0%

: 128-44-9
saccharin sodium salt

: 585-71-7,38661-81-3
(1-bromoethyl)benzne

: 41335-50-6
3-oxo-N-(1-phenylethyl)benzo[d]isothiazole-2(3h)sulfonamide 1,1-dioxide

Guidance literature:: In N,N-dimethyl-formamide; at 90 ℃;
DOI:10.1002/ejoc.200600508

Reference yield: 24.0%

: 98-85-1,13323-81-4
1-Phenylethanol

: 81-07-2
saccharin

: 1467118-16-6
3-(1-phenylethyloxy)-1,2-benzisothiazole 1,1-dioxide

: 41335-50-6
3-oxo-N-(1-phenylethyl)benzo[d]isothiazole-2(3h)sulfonamide 1,1-dioxide

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; regioselective reaction;
DOI:10.3184/174751913X13716447161975