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Trimethyl(2-methylbut-3-yn-2-yl)silane is an organosilicon compound with the molecular formula C?H??Si. It features a silicon atom bonded to three methyl groups and a 2-methylbut-3-yn-2-yl group, which is a branched alkyne with a terminal triple bond and a methyl group on the second carbon. This structure endows the compound with unique properties, such as reactivity towards electrophiles due to the presence of the triple bond, and potential applications in organic synthesis and as a protecting group in chemical reactions. The compound's stability and reactivity can be influenced by the steric and electronic effects of the substituents around the silicon and the triple bond.

81358-51-2

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81358-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81358-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,5 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81358-51:
(7*8)+(6*1)+(5*3)+(4*5)+(3*8)+(2*5)+(1*1)=132
132 % 10 = 2
So 81358-51-2 is a valid CAS Registry Number.

81358-51-2Relevant academic research and scientific papers

Ene Reactions of Allylic Derivatives of Silicon, Germanium, Tin and Lead with N-Phenyltriazolinedione: the Effect of Varying the Metal

Cai, Jiaqiang,Davies, Alwyn G.

, p. 1743 - 1746 (2007/10/02)

The compounds Ph3MCH2CH=CH2 and (M=Si, Ge, Sn or Pb) have been treated with 4-phenyl-1,2,4-triazoline-3,5-dione, and the relative yields of the products of the M-ene reaction, of the H-ene reaction, and of the reaction involving cycloaddition with shift of the organometallic substituent, have been determined.The silicon compounds react principally by the H-ene process.The cycloaddition process is at a maximum (50percent or 70percent) with the germanium compounds, and the tin compounds show mainly the M-ene reaction, with some cycloaddition but no H-ene reaction.Triphenylprop-2-enylplumbane show only the M-ene reaction.In trimethyl(1,1-dimethylprop-2-enyl)silane, in which the H-ene reaction is blocked, only cycloaddition with shift of the silyl group is observed.

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