73842-99-6 Usage
Description
3-(T-BUTYLDIMETHYLSILOXY)PROPANOL, also known as 3-((tert-Butyldimethylsilyl)oxy)-propanol or 3-[(tert-butyldimethylsilyl)oxy]-1-propanol, is an intermediate compound formed during the synthesis of 3-(tert-butyldimethylsilyl)oxy]propanal. It is characterized by its clear, colorless liquid appearance.
Uses
Used in Chemical Synthesis:
3-(T-BUTYLDIMETHYLSILOXY)PROPANOL is used as an intermediate compound for the synthesis of 3-(tert-butyldimethylsilyl)oxy]propanal. Its role in this process is crucial for the production of the final product, which may have various applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(T-BUTYLDIMETHYLSILOXY)PROPANOL may be used as a building block for the development of new drugs or drug candidates. Its unique chemical structure could potentially be utilized in the creation of novel therapeutic agents.
Used in Research and Development:
3-(T-BUTYLDIMETHYLSILOXY)PROPANOL can also be employed in research and development settings, where it may be used to study its chemical properties, reactivity, and potential applications in various fields, including materials science, chemical engineering, and biotechnology.
Used in Material Science:
In the field of material science, 3-(T-BUTYLDIMETHYLSILOXY)PROPANOL could be used as a component in the development of new materials with specific properties, such as improved stability, reactivity, or biocompatibility.
Check Digit Verification of cas no
The CAS Registry Mumber 73842-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73842-99:
(7*7)+(6*3)+(5*8)+(4*4)+(3*2)+(2*9)+(1*9)=156
156 % 10 = 6
So 73842-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H22O2Si/c1-9(2,3)12(4,5)11-8-6-7-10/h10H,6-8H2,1-5H3
73842-99-6Relevant articles and documents
Functional analysis of an aspartate-based epoxidation catalyst with amide-to-alkene peptidomimetic catalyst analogues
Jakobsche, Charles E.,Peris, Gorka,Miller, Scott J.
supporting information; experimental part, p. 6707 - 6711 (2009/03/12)
Subtle exchange: Replacement of an amide function with alkene or fluoroalkene groups provides a new class of epoxidation catalysts (see scheme). The structure-dependent catalytic behavior of these isosteric peptides provides mechanistic insights in their mode of action. (Chemical Equation Presented).
A remarkable solvent effect toward the Pd/C-catalyzed cleavage of silyl ethers
Sajiki, Hironao,Ikawa, Takashi,Hattori, Kazuyuki,Hirota, Kosaku
, p. 654 - 655 (2007/10/03)
Selective hydrogenation conditions of olefin, benzyl ether and acetylene functionalities in the presence of TBDMS or TES ether have been developed.
Selective acceleration for deprotection of benzyl ethers with ti-HMS
Itoh, Akichika,Kodama, Tomohiro,Maeda, Shiro,Masaki, Yukio
, p. 9461 - 9464 (2007/10/03)
Ti-HMS, a Ti-loaded hexagonal mesoporous silica, was found to accelerate deprotection of benzyl ethers under hydrogenolytic conditions with palladium catalyst. Such acid-sensitive functional groups as silyl ether and acetal moieties in the molecule were little affected by Ti-HMS, which possesses Lewis acid sites due to Ti-atom.
