6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione

Base Information

Chemical Name:6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione
CAS No.:33665-93-9
Molecular Formula:C9H7NO4S
Molecular Weight:225.225
Hs Code.:
DSSTox Substance ID:DTXSID80537460
Wikidata:Q82412452

Synonyms:33665-93-9;SCHEMBL3183012;DTXSID80537460;6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione

Suppliers and Price of 6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione

Supply Marketing:

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

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Chemical Property of 6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:225.00957888
Heavy Atom Count:15
Complexity:387

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC(=O)NS(=O)(=O)O2

Technology Process of 6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione

There total 1 articles about 6-Phenyl-2H-1,2lambda~6~,3-oxathiazine-2,2,4(3H)-trione 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:

: 1495-51-8
fluorosulfonyl isocyanate

: 536-74-3
phenylacetylene

: 33665-93-9
2,2-dioxo-6-phenyl-2,3-dihydro-2λ⁶-[1,2,3]oxathiazin-4-one

Guidance literature:: Multistep reaction; (i), (ii) aq. Na₂CO₃;
DOI:10.1016/S0040-4039(01)97655-5

Reference yield: 76.0%

: 33665-93-9
2,2-dioxo-6-phenyl-2,3-dihydro-2λ⁶-[1,2,3]oxathiazin-4-one

: 72827-13-5
4-Chloro-6-phenyl-[1,2,3]oxathiazine 2,2-dioxide

Guidance literature:: With phosphorus pentachloride; In tetrachloromethane; Heating;

Reference yield:

: 33665-93-9
2,2-dioxo-6-phenyl-2,3-dihydro-2λ⁶-[1,2,3]oxathiazin-4-one

: 72811-88-2
(Z)-3-anilino-3-phenylprop-2-enenitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / PCl₅ / CCl₄ / Heating

2: triethylamine, 4-dimethylaminopyridine / CH₂Cl₂ / 12 h / Ambient temperature

With dmap; phosphorus pentachloride; triethylamine; In tetrachloromethane; dichloromethane;