Tetraphenylantimony(V) methoxide

Base Information

Chemical Name:Tetraphenylantimony(V) methoxide
CAS No.:14090-94-9
Molecular Formula:C25H23 O Sb
Molecular Weight:461.207
Hs Code.:2931900090
European Community (EC) Number:683-354-4
Mol file:14090-94-9.mol

Synonyms:Tetraphenylantimony(V) methoxide;Tetraphenylantimony methoxide;methoxy(tetraphenyl)-lambda5-stibane;14090-94-9;methoxytetraphenylantimony

Suppliers and Price of Tetraphenylantimony(V) methoxide

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 Tetraphenylantimony(V) methoxide

Chemical Property:

Melting Point:202-218 °C(lit.)
PSA：23.06000
LogP:6.21890
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:460.07870
Heavy Atom Count:27
Complexity:367

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

Safty Information:

Pictogram(s):
Hazard Codes:Xn,N
Statements: 20/22-51/53
Safety Statements: 61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CO[Sb](C1=CC=CC=C1)(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of Tetraphenylantimony(V) methoxide

There total 2 articles about Tetraphenylantimony(V) methoxide 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: 90.0%

: 16894-69-2,21450-52-2
tetraphenylstibonium bromide

: 124-41-4
sodium methylate

: 14090-94-9
methoxytetraphenylstibane

Guidance literature:: In methanol; reagents were dissolved in MeOH and refluxed for 1 h; soln. was cooled to room temp., cold water was slowly added with stirring, ppt. was removed, washed with cold water and dried in vac.; NMR;
DOI:10.1021/ja00274a059