79239-05-7 Usage
Uses
Used in Materials Science:
TRIMETHYL-((E)-3-PHENYL-BUT-2-ENYL)-SILANE is used as a reagent in the synthesis of functionalized silicon compounds, contributing to the development of new materials with specialized properties and functions.
Used in Pharmaceutical Industry:
TRIMETHYL-((E)-3-PHENYL-BUT-2-ENYL)-SILANE is used as an intermediate in the preparation of silane-containing compounds for pharmaceutical applications, potentially enhancing the properties and functions of drug molecules.
Used in Agrochemicals:
TRIMETHYL-((E)-3-PHENYL-BUT-2-ENYL)-SILANE is used as a building block in the design and development of new silicon-based agrochemicals, improving the efficiency and selectivity of these compounds in agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 79239-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79239-05:
(7*7)+(6*9)+(5*2)+(4*3)+(3*9)+(2*0)+(1*5)=157
157 % 10 = 7
So 79239-05-7 is a valid CAS Registry Number.
79239-05-7Relevant academic research and scientific papers
Carbonium Ion Rearrangements Controlled by the Presence of a Silyl Group
Fleming, Ian,Patel, Shailesh K.,Urch, Christopher J.
, p. 115 - 124 (2007/10/02)
γ-Silyl tertiary alcohols rearrange in protic acid with 1,2-shift of hydride, phenyl, or alkyl groups, and loss of the silyl group to give alkenes.The placing of the silyl group thus controls the carbonium ion rearrangement in a preparatively useful way.Methoxycarbonyl groups do not migrate; instead, cyclopropanes are formed, except when the conformation suitable for cyclopropane formation is unattainable.When the alkene product is 2,2-disubstituted, it can be reprotonated under the reaction conditions and does not therefore always survive.This can be avoided by carrying out the reaction using a Lewis acid on the silyl ether.The starting γ-silyl alcohols are prepared by a variety of versatile methods.
