Oxo bis[triphenyl(chloro)anti mony]

Base Information

Chemical Name:Oxo bis[triphenyl(chloro)anti mony]
CAS No.:1538-63-2
Molecular Formula:C₃₆H₃₀Cl₂OSb₂
Molecular Weight:793.04
Hs Code.:
DSSTox Substance ID:DTXSID801296363
NSC Number:117315
Mol file:1538-63-2.mol

Synonyms:1538-63-2;oxo bis[triphenyl(chloro)anti mony];DTXSID801296363;NSC117315;NSC-117315;Dichloro-I(1/4)-oxohexaphenyldiantimony

Suppliers and Price of Oxo bis[triphenyl(chloro)anti mony]

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 9 raw suppliers

Chemical Property of Oxo bis[triphenyl(chloro)anti mony]

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:791.97540
Heavy Atom Count:41
Complexity:664

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)[Sb](C2=CC=CC=C2)(C3=CC=CC=C3)(O[Sb](C4=CC=CC=C4)(C5=CC=CC=C5)(C6=CC=CC=C6)Cl)Cl

Technology Process of Oxo bis[triphenyl(chloro)anti mony]

There total 1 articles about Oxo bis[triphenyl(chloro)anti mony] 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:

: 603-36-1
triphenylantimony

: silver(I) chloride

: 106436-42-4,115730-70-6,1538-63-2
μ-oxobis(chlorotriphenylantimony(V))benzene solvate (1/2)

Guidance literature:: In acetonitrile; mixing (SbPh3 : AgCl = 3 : 1);
DOI:10.1071/C96042

Reference yield: 80.0%

: 3425-46-5
potassium selenocyanate

: 1538-63-2,115730-70-6,106436-42-4
μ-oxy-bis(triphenylantimony) dichloride

: μ-oxy-bis(triphenylantimony) bis-selenocyanate

Guidance literature:: With catalyst: 18-crown-6; In benzene; byproducts: KCl; stirring antimony complex and KSeCN in benzene at room temp. in the presence of catalytic amt. of 18-crown-6 for 4-6 h; filtration; removal of solvent in vac.; recrystn. from petroleum ether;elem. anal.;
DOI:10.1016/S0277-5387(00)84561-1