1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-

Base Information

Chemical Name:1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-
CAS No.:61379-07-5
Molecular Formula:C17H15NO2S
Molecular Weight:297.378
Hs Code.:
DSSTox Substance ID:DTXSID10486452
Wikidata:Q82327312

Synonyms:61379-07-5;1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-;DTXSID10486452

Suppliers and Price of 1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-

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 0 raw suppliers

Chemical Property of 1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:297.08234989
Heavy Atom Count:21
Complexity:396

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CSC(=C(O1)C2=CC=CC=C2)C(=O)NC3=CC=CC=C3

Technology Process of 1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl-

There total 1 articles about 1,4-Oxathiin-3-carboxamide, 5,6-dihydro-N,2-diphenyl- 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:

: 61379-07-5
2-phenyl-5,6-dihydro-[1,4]oxathiine-3-carboxylic acid anilide

Guidance literature:: 2-Phenyl-1,4-oxathien-(2)-3-carbonsaeure 1. SOCl2 2. Anilin;

Reference yield:

: 61379-07-5
2-phenyl-5,6-dihydro-[1,4]oxathiine-3-carboxylic acid anilide

: 959-66-0
3-oxo-3-phenylpropionanilide

Guidance literature:: Multi-step reaction with 2 steps

1: chlorine / tetrahydrofuran; CH₂Cl₂ / Ambient temperature

2: 60 percent sodium hydride in oil / tetrahydrofuran / Ambient temperature

With chlorine; sodium hydride; In tetrahydrofuran; dichloromethane;
DOI:10.3987/COM-98-S(H)61