Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-

Base Information

Chemical Name:Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-
CAS No.:142799-36-8
Molecular Formula:C30H46F2Sn
Molecular Weight:563.402
Hs Code.:
DSSTox Substance ID:DTXSID10463602
Wikidata:Q82288567

Synonyms:Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-;142799-36-8;DTXSID10463602

Suppliers and Price of Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-

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 1 raw suppliers

Chemical Property of Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:564.258960
Heavy Atom Count:33
Complexity:508

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1=CC(=C(C(=C1)C(C)C)[Sn](C2=C(C=C(C=C2C(C)C)C(C)C)C(C)C)(F)F)C(C)C

Technology Process of Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]-

There total 1 articles about Stannane, difluorobis[2,4,6-tris(1-methylethyl)phenyl]- 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%

: 98539-88-9
hexakis(2,4,6-triisopropylphenyl)cyclotristannoxane

: 142799-36-8
bis(2,4,6-triisopropylphenyl)difluorostannane

Guidance literature:: With hydrogen fluoride; In benzene; to a soln. of Sn compound added aq. HF, stirred (2 h, room temp.); evapn. (vac.), pentane add., dried (Na2SO4), solvent removed in vac., crystn. (pentane) or distn. (1 Torr, 170°C); elem. anal.;
DOI:10.1021/om00044a005

Reference yield: 100.0%

: 142799-36-8
bis(2,4,6-triisopropylphenyl)difluorostannane

: 214424-22-3
tetraphosphanylsilane

: 670237-45-3
bis(2,4,6-triisopropylphenyl)SnFPH₂

Guidance literature:: In benzene; byproducts: FSi(PH2)3; NMR;
DOI:10.1039/b308660g

Reference yield: 80.0%

: 142799-36-8
bis(2,4,6-triisopropylphenyl)difluorostannane

: 136965-63-4
P(H₂)(C₆H₂(CH₃)3)W(CO)5

: 211488-38-9
(C₆H₂(CH(CH₃)2)3)2SnFP(H)(C₆H₂(CH₃)3)W(CO)5

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; pentane; high vac. technique; Li-compd. soln. (hexane) addn. to P-compd. soln. (THF) at -78°C, stirring at this temp. for 0.5 h, Sn-compd. soln. (pentane, -78°C) addn., mixt. allowing to reach room temp., Li-salts removal; residue recrystn. (pentane);
DOI:10.1080/10426509708043555