1730-67-2 Usage
Uses
Used in Pharmaceutical Synthesis:
Acetaldehyde, (triphenylsilyl)is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique reactivity and properties facilitate the production of complex organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, Acetaldehyde, (triphenylsilyl)serves as an essential intermediate for the synthesis of various agrochemicals. Its application aids in the development of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Fine Chemicals Synthesis:
Acetaldehyde, (triphenylsilyl)is also employed in the synthesis of fine chemicals, which are high-purity specialty chemicals used in various industries, including fragrances, dyes, and advanced materials. Its unique properties enable the production of high-quality fine chemicals with specific applications.
As a Stable Compound for Inert Conditions:
Due to its stability, Acetaldehyde, (triphenylsilyl)is generally handled and stored under inert conditions to prevent decomposition or unwanted reactions. This characteristic ensures the preservation of its properties and reactivity, making it suitable for use in sensitive chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 1730-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1730-67:
(6*1)+(5*7)+(4*3)+(3*0)+(2*6)+(1*7)=72
72 % 10 = 2
So 1730-67-2 is a valid CAS Registry Number.
1730-67-2Relevant academic research and scientific papers
Sato, Susumu,Matsuda, Isamu,Izumi, Yusuke
, p. 4229 - 4230 (1985)
The transfer hydrogenation of β-trimethylsilyl alcohols catalyzed by HRh(PPh3)4 has been successfully applied to the efficient synthesis of α-trimethylsilyl ketones.
Reactions of (triphenylsilyl)ethylene oxide with Grignard reagents (and with MgBr2). A reinvestigation
Hudrlik, Paul F.,Ahmed, Mohamed E.,Roberts, Ralph R.,Hudrlik, Anne M.
, p. 4395 - 4399 (2007/10/03)
Reactions of (triphenylsilyl)ethylene oxide (1) with simple Grignard reagents such as EtMgBr and PhMgBr have been reported to yield crystalline hydroxysilanes assigned as the α-hydroxy silanes expected from β opening of the epoxide. Reinvestigation of these reactions showed that the hydroxysilanes were the β-hydroxy silanes 4 and 7 expected from a rearrangement-trapping sequence; a bromohydrin, assigned as the α-bromo-β-hydroxy silane 9 from α opening, and (triphenylsilyl)acetaldehyde (8) were also formed.
A regiodefined synthesis of α-trimethylsilyl ketones catalyzed by rhodium(I) hydride complex
Sato, Susumu,Matsuda, Isamu,Izumi, Yusuke
, p. 71 - 88 (2007/10/02)
Regiodefined synthesis of α-trimethylsilyl ketones is attained by one of three different routes: isomerization of β-trimethylsilyl allyl alcohols (route A), isomerization of β'-trimethylsilyl allyl alcohols (route B), and dehydrogenation of β-trimethylsil
