TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96

Base Information

Chemical Name:TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96
CAS No.:149013-84-3
Molecular Formula:C₁₆H₂₂SiSn
Molecular Weight:361.146
Hs Code.:29310099
Mol file:149013-84-3.mol

Synonyms:TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96

Suppliers and Price of TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 6 raw suppliers

Chemical Property of TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96

Chemical Property:

Boiling Point:125-130°C
PSA：0.00000
LogP:3.29600

Purity/Quality:: 98%min ^*data from raw suppliers

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Technology Process of TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96

There total 2 articles about TRIMETHYLSTANNYLMETHYLDIPHENYLSILAN, 96 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:

: 117309-69-0
ClMgCH₂SiH(C₆H₅)2

: 1066-45-1
trimethyltin(IV)chloride

: 149013-84-3
(CH₃)3SnCH₂SiH(C₆H₅)2

Guidance literature:: In diethyl ether; byproducts: MgCl2; under anaerobic and anhydrous conditions, soln. of Grignard compd. is added to soln. of Me3SnCl, mixt. is stirred for 5 min; volatiles are removed in vac., product is extd. with pentane, removal of solvent;

Reference yield:

: (η5-C5Me5)(P(isopropyl)3)Ru(H)(η2-CH2Si(C6H5)2)

: 1066-45-1
trimethyltin(IV)chloride

: (η5-C5Me5)Ru(P(i-Pr)3)Cl

: 149013-84-3
(CH₃)3SnCH₂SiH(C₆H₅)2

Guidance literature:: In benzene-d6; under anaerobic and anhydrous conditions, soln. of Me3SnCl is added to soln. of the complex at -78°C, mixt. is stirred for 2 h at same temp., then mixt. is warmed to room temp.; monitored by (1)H-NMR spectroscopy;