Stannyloxy,1,1,1-tributyl-

Base Information

Chemical Name:Stannyloxy,1,1,1-tributyl-
CAS No.:1067-97-6
Molecular Formula:C12H28 O Sn
Molecular Weight:307.064
Hs Code.:
Mol file:1067-97-6.mol

Synonyms:Stannyloxy,1,1,1-tributyl-;SCHEMBL932356

Suppliers and Price of Stannyloxy,1,1,1-tributyl-

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 Stannyloxy,1,1,1-tributyl-

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:9
Exact Mass:308.116218
Heavy Atom Count:14
Complexity:72.1

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s): Moderately toxic. TWA 0.1 mg(Sn)/m³; STEL 0.2 mg(Sn)/m³ (skin).
Hazard Codes:Moderately toxic. TWA 0.1 mg(Sn)/m3; STEL 0.2 mg(Sn)/m3 (skin).

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC[Sn+](CCCC)CCCC.[OH-]

Technology Process of Stannyloxy,1,1,1-tributyl-

There total 38 articles about Stannyloxy,1,1,1-tributyl- 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: 75.0%

: 24850-33-7
allyltributylstanane

: 109-63-7
trifluoroborane diethyl ether

: 123-38-6
propionaldehyde

: 1067-97-6
tributyltin hydroxide

: 130268-46-1
4-hydroxy-2,6-diethyltetrahydropyran

Guidance literature:: In neat (no solvent); (N2); addn. of Sn-compd. to 1 equiv. of BF3OEt2 and 1 equiv. of EtCOH at -15°C, warming to room temperature; treatment with sat. aq. NH4Cl;
DOI:10.1016/0022-328X(90)85025-T