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Tributyl(trimethylsilylmethyl)tin

Base Information Edit
  • Chemical Name:Tributyl(trimethylsilylmethyl)tin
  • CAS No.:77425-85-5
  • Molecular Formula:C16H38 Si Sn
  • Molecular Weight:377.273
  • Hs Code.:2931900090
  • DSSTox Substance ID:DTXSID60504796
  • Wikidata:Q82359541
  • Mol file:77425-85-5.mol
Tributyl(trimethylsilylmethyl)tin

Synonyms:Tributyl(trimethylsilylmethyl)tin;77425-85-5;Tri-n-butyl(trimethylsilylmethyl)tin;Trimethyl(tributylstannylmethyl)silane;(Trimethylsilylmethyl)tri-n-butyltin;trimethyl[(tributylstannyl)methyl]silane;trimethyl((tributylstannyl)methyl)silane;DTXSID60504796;Tri-n-butyl(trimethylsilymethyl)tin;3-Bromonaphthalene-1-carboxylicacid;AKOS025293636;(tributylstannyl)( trimethylsilyl)methane;FT-0730363;T1866;EN300-18532813

Suppliers and Price of Tributyl(trimethylsilylmethyl)tin
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • TRI-N-BUTYL(TRIMETHYLSILYLMETHYL)TIN 95.00%
  • 5G
  • $ 893.31
Total 10 raw suppliers
Chemical Property of Tributyl(trimethylsilylmethyl)tin Edit
Chemical Property:
  • Boiling Point:146°C/2.5mmHg 
  • PSA:0.00000 
  • LogP:6.71290 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:11
  • Exact Mass:378.176480
  • Heavy Atom Count:18
  • Complexity:174
Purity/Quality:

98%Min *data from raw suppliers

TRI-N-BUTYL(TRIMETHYLSILYLMETHYL)TIN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 20/21/22-36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCC[Sn](CCCC)(CCCC)C[Si](C)(C)C
Technology Process of Tributyl(trimethylsilylmethyl)tin

There total 3 articles about Tributyl(trimethylsilylmethyl)tin 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:
Guidance literature:
With iodine; ammonium chloride; In diethyl ether; N2-atmosphere; addn. of Me3SiCH2Cl to Mg (activated with I2), refluxing(1 h), addn. of Bu3SnCl, refluxing (18 h); addn. of satd. aq. NH4Cl, extn. of aq. layer (ether), washing of org. layer (satd. aq. NaCl), drying (Na2SO4), evapn. of ether, distn. (vac.);
DOI:10.1021/om00140a026
Guidance literature:
With n-butyllithium; In diethyl ether; hexane; treatment of BuLi in hexane with teluride in THF (-78°C), addn. of Me3SiCl, warming to room temp. (mixing, over period of 1 h); not isolated; NMR spectroscopy;
DOI:10.1021/om00118a086
Guidance literature:
In benzene-d6; (N2); to soln. of scandium complex in C6D6 was added nBu3SnCl, allowed for 17 h; detected by NMR;
DOI:10.1021/ja204209t
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