2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide

Base Information

Chemical Name:2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide
CAS No.:2346-86-3
Molecular Formula:C15H11NO5S
Molecular Weight:317.322
Hs Code.:
DSSTox Substance ID:DTXSID80367264
Wikidata:Q82152999
Mol file:2346-86-3.mol

Synonyms:2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide;2346-86-3;Oprea1_128051;Oprea1_607129;DTXSID80367264;STK047605;AKOS003224929;SR-01000213956;SR-01000213956-1

Suppliers and Price of 2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide

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 1 raw suppliers

Chemical Property of 2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:317.03579362
Heavy Atom Count:22
Complexity:547

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 1,1-dioxide

There total 5 articles about 2-(phenoxyacetyl)-1,2-benzothiazol-3(2H)-one 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: 95.0%

: 701-99-5
Phenoxyacetyl chloride

: 81-07-2
saccharin

: 2346-86-3
2-phenoxyacetyl-3-oxo-4,5-benzo-1,2-thiazoline 1,1-dioxide

Guidance literature:: With triethylamine; In dichloromethane; for 0.5h; Ambient temperature;

Reference yield: 83.0%

: 96658-28-5
diethyl 2-(3-oxo-2,3-dihydro-1,2-benzisosulfonazolyl)phosphonate

: 122-59-8
2-phenoxyacetic acid

: 2346-86-3
2-phenoxyacetyl-3-oxo-4,5-benzo-1,2-thiazoline 1,1-dioxide

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1246/cl.1985.123

Reference yield:

: 81-07-2
saccharin

: 2346-86-3
2-phenoxyacetyl-3-oxo-4,5-benzo-1,2-thiazoline 1,1-dioxide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

2: 83 percent / Et₃N / CH₂Cl₂

With triethylamine; In dichloromethane;
DOI:10.1246/cl.1985.123