Triphenyl(salicyloyloxy)stannane

Base Information

Chemical Name:Triphenyl(salicyloyloxy)stannane
CAS No.:24379-26-8
Molecular Formula:C25H20 O3 Sn
Molecular Weight:487.142
Hs Code.:2918230000
European Community (EC) Number:246-212-9
UNII:3QJX8T3JA6
DSSTox Substance ID:DTXSID20179126
Mol file:24379-26-8.mol

Synonyms:TPS compound;triphenyltin salicylate

Suppliers and Price of Triphenyl(salicyloyloxy)stannane

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 6 raw suppliers

Chemical Property of Triphenyl(salicyloyloxy)stannane

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：60.36000
Density:g/cm³
LogP:4.80510
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:488.043447
Heavy Atom Count:29
Complexity:473

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)OC(=O)C4=CC=CC=C4O

Technology Process of Triphenyl(salicyloyloxy)stannane

There total 3 articles about Triphenyl(salicyloyloxy)stannane 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: 88.0%

: 1262-21-1
bis(triphenyltin) oxide

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 24379-26-8
2-hydroxybenzoatotriphenyltin(IV)

Guidance literature:: In benzene; byproducts: H2O; reflux, 30 min; distg. off benzene and H2O, dissolving oily residue in Et2O, adding hexane, crystg. by placing in refrigerator overnight; elem. anal.;

Reference yield: 81.0%

: 76-87-9
triphenyltin(IV) hydroxide

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 24379-26-8
2-hydroxybenzoatotriphenyltin(IV)

Guidance literature:: In toluene; byproducts: H2O; (inert atm.); mixture of tin compound and 2-hydroxybenzoic acid was reflux in toluene for 4-6 h with Dean-Stark apparatus, stand in room temp.; solvent evapd. in vac., recrystallized in chloroform/n-hexane (3:1), elem. anal.;
DOI:10.1016/j.jorganchem.2008.06.027

Reference yield:

: 159113-64-1
triphenyl(4-t-butylphenoxo)tin(IV)

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 24379-26-8
2-hydroxybenzoatotriphenyltin(IV)

Guidance literature:: In benzene; mixt. refluxed, resulting solid washed with petroleum ether; resulting solid washed with petroleum ether, dried under reduced pressure, elem. anal.;