2917-47-7 Usage
Description
3-(Trimethylsilyl)-1-propanol, also known as (3-Trimethylsilyl)propan-1-ol, is a clear, colorless liquid with unique chemical properties. It is an organosilicon compound that features a trimethylsilyl group attached to a propanol molecule, which contributes to its distinct reactivity and applications in various chemical processes.
Uses
Used in Polymer Synthesis:
3-(Trimethylsilyl)-1-propanol is used as a reagent in the synthesis of telechelic oligomers via atom transfer radical polymerization (ATRP) of styrene. Its unique chemical properties enable the formation of well-defined oligomers with controlled molecular weights and architectures, which are essential for various applications in materials science and engineering.
Used in Organic Synthesis:
In the field of organic synthesis, 3-(Trimethylsilyl)-1-propanol is used as a precursor for the preparation of β-seleno-γ-silyl alcohols. These compounds are valuable intermediates in the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries, due to their unique reactivity and functional group compatibility.
Used in Chemical Research:
3-(Trimethylsilyl)-1-propanol is also utilized in chemical research as a model compound for studying the reactivity and properties of organosilicon compounds. Its clear, colorless liquid form and unique chemical structure make it an ideal candidate for investigating various reaction mechanisms and exploring new synthetic methodologies.
Used in the Pharmaceutical Industry:
3-(Trimethylsilyl)-1-propanol can be employed as a building block or intermediate in the synthesis of pharmaceutical compounds, particularly those involving organosilicon moieties. Its unique properties may contribute to the development of novel drugs with improved pharmacological profiles and therapeutic applications.
Used in the Electronics Industry:
Due to its organosilicon nature, 3-(Trimethylsilyl)-1-propanol may find applications in the electronics industry, particularly in the development of new materials for semiconductors, sensors, and other electronic devices. Its unique chemical properties could potentially enhance the performance and functionality of these materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2917-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2917-47:
(6*2)+(5*9)+(4*1)+(3*7)+(2*4)+(1*7)=97
97 % 10 = 7
So 2917-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H16OSi/c1-8(2,3)6-4-5-7/h7H,4-6H2,1-3H3
2917-47-7Relevant articles and documents
Synthesis of 1-silabicyclo[4.4.0]dec-5-en-4-ones: A model of the A and B rings of 10-silatestosterone
Diez-Gonzalez, Silvia,Paugam, Renee,Blanco, Luis
body text, p. 3298 - 3307 (2009/04/07)
1-Silabicyclo[4.4.0]dec-5-en-4-ones, a novel type of organosilicon compound, have been prepared from 2-methylidene-1-(3-oxopropyl)-1- silacyclohexanes by an ene reaction as the key transformation. Various routes to the starting aldehydes from 3-halopropyl, allyl, or 3-(4-methoxybenzyloxy) propylsilanes have been investigated. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
REGIO- AND STEREOSELECTIVE SYNTHESIS OF ALLYLTRIMETHYLSILANES VIA KRIEF-REICH ELIMINATION IN β-SELENO-γ-SILYL ALCOHOLS
Sarkar, Tarun K.,Ghosh, Sunil K.,Satapathi, Tushar K.
, p. 1885 - 1898 (2007/10/02)
The synthesis of (E)-allyltrimethylsilanes by regio- and stereocontrolled pathways is described based on the preference for Krief-Reich elimination over silicon-controlled rearrangement in β-seleno-γ-silyl alcohols, readily available from α-selenoaldehydes, 10 - 12.Usefulness of this protocol for the introduction of the allylsilane function α to the carbonyl group in cycloalkanones as well as for the preparation of unsymmetrically substituted allylsilanes is also reported.
Organoborane-Catalyzed Hydroalumination of Olefins
Maruoka, Keiji,Sano, Hiromi,Shinoda, Kiyotaka,Nakai, Shuichi,Yamamoto, Hisashi
, p. 6036 - 6038 (2007/10/02)
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