5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane

Base Information

Chemical Name:5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane
CAS No.:112995-73-0
Molecular Formula:C₁₀H₁₂NO₃S₂Sb
Molecular Weight:380.092
Hs Code.:
DSSTox Substance ID:DTXSID90587193
Wikidata:Q82479541

Synonyms:112995-73-0;5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane;DTXSID90587193

Suppliers and Price of 5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane

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 5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:378.92967
Heavy Atom Count:17
Complexity:248

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CS[Sb](SCCO1)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane

There total 1 articles about 5-(4-Nitrophenyl)-1,4,6,5-oxadithiastibocane 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: 45.0%

: 112995-72-9
4-nitrophenyldichlorostibine

: 2150-02-9
bis(2-mercaptoethyl)ether

: 112995-73-0
5-p-nitrophenyl-1-oxa-4,6-dithia-5-stibocane

Guidance literature:: With (C₂H₅)3N; In toluene; byproducts: (C2H5)3N*HCl; toluene soln. of p-NO2C6H4SbCl2 added dropwise over 2 h to toluene soln. of (HSCH2CH2)2O and Et3N at room temp. with stirring under dry Ar, stirred for many hours; Et3N*HCl sepd., cooled to -20°C, left standing overnight, sucked off, further crop of product crystd. from mother liquor by concn. with rotary evaporator, recrystd. from toluene; elem. anal.;
DOI:10.1016/0022-328X(87)85051-9