Stannane, 1,5-pentanediylbis[trichloro-

Base Information

Chemical Name:Stannane, 1,5-pentanediylbis[trichloro-
CAS No.:351387-98-9
Molecular Formula:C5H10Cl6Sn2
Molecular Weight:520.272
Hs Code.:
DSSTox Substance ID:DTXSID50464613
Wikidata:Q82290010

Synonyms:Stannane, 1,5-pentanediylbis[trichloro-;351387-98-9;1,5-Bis(trichlorostannyl)pentane;DTXSID50464613

Suppliers and Price of Stannane, 1,5-pentanediylbis[trichloro-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Stannane, 1,5-pentanediylbis[trichloro-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:4
Exact Mass:519.69223
Heavy Atom Count:13
Complexity:123

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(CC[Sn](Cl)(Cl)Cl)CC[Sn](Cl)(Cl)Cl

Technology Process of Stannane, 1,5-pentanediylbis[trichloro-

There total 1 articles about Stannane, 1,5-pentanediylbis[trichloro- 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%

: 5588-71-6
1,5-bis(triphenylstannyl)pentane

: 7646-78-8
tin(IV) chloride

: 351387-98-9
1,5-bis(trichlorostannyl)pentane

: 1124-19-2
phenyltin trichloride

Guidance literature:: In neat (no solvent); heating for 3 h at 120-130°C; the mixt. was distd. in vac.; elem. anal.;
DOI:10.1021/om010202j

Reference yield: 79.0%

: 351387-98-9
1,5-bis(trichlorostannyl)pentane

: 536-74-3
phenylacetylene

: 476014-63-8
1,4-bis(tris(phenylethynyl)stannyl)pentane

Guidance literature:: With n-butyl lithium; In toluene; byproducts: LiCl; to a soln. of propyne in toluene at -78°C was slowly added a soln. of butyllithium in hexanes, after 15 min stirring at room temp., a soln. of Sn-compound in toluene was added at -78°C, hexated at 70°C for 12 h (N2); filtered on dry MgSO4 under dry N2, toluene was evapd., recrystd. from toluene; elem. anal.;
DOI:10.1021/om0202468