Stannane, 1,4-naphthalenediylbis(trimethyl-

Base Information

Chemical Name:Stannane, 1,4-naphthalenediylbis(trimethyl-
CAS No.:76246-38-3
Molecular Formula:C16H24 Sn2
Molecular Weight:453.78
Hs Code.:2931900090
DSSTox Substance ID:DTXSID40227113
Wikidata:Q83106761
Mol file:76246-38-3.mol

Synonyms:76246-38-3;Stannane, 1,4-naphthalenediylbis(trimethyl-;DTXSID40227113;1,4-Bis-(trimethylstannyl)naphthalene;FT-0741974;Stannane, 1,4-naphthalenediylbis[trimethyl-]-

Suppliers and Price of Stannane, 1,4-naphthalenediylbis(trimethyl-

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
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price

Total 5 raw suppliers

Chemical Property of Stannane, 1,4-naphthalenediylbis(trimethyl-

Chemical Property:

Vapor Pressure:1.18E-05mmHg at 25°C
Boiling Point:380.6°C at 760 mmHg
Flash Point:188°C
PSA：0.00000
LogP:3.93020
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:453.99161
Heavy Atom Count:18
Complexity:255

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Sn](C)(C)C1=CC=C(C2=CC=CC=C21)[Sn](C)(C)C

Technology Process of Stannane, 1,4-naphthalenediylbis(trimethyl-

There total 2 articles about Stannane, 1,4-naphthalenediylbis(trimethyl- 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: 10.0%

: 1066-45-1
trimethyltin(IV)chloride

: 76246-38-3
1,4-bis(trimethylstannyl)naphthalene

Guidance literature:: With magnesium; 1,4-dihalogenonaphthalene; In tetrahydrofuran; the aromatic halogeno-compd. was added to the soln. of Mg and trimethylchloro-compd., refluxed for several d; hydrolysed with dild. HCl, extd. with ether, dried over Na2SO4, the solvent evapd., the product recrystd. from methanol; elem. anal.;