18171-24-9 Usage
Uses
Used in Organic Synthesis:
3-((chloroMethyl)diMethylsilyl)propan-1-ol is utilized as a reagent for the introduction of the trimethylsilyl group into various organic molecules. Its ability to act as a protective group for alcohols in organic synthesis is particularly valuable, as it helps prevent unwanted side reactions during the synthesis process.
Used in Pharmaceutical and Agrochemical Preparation:
3-((chloroMethyl)diMethylsilyl)propan-1-ol serves as a fundamental building block in the preparation of a variety of pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to the development of new and effective compounds for medical and agricultural applications.
Used in Chemical Reactions:
The presence of the chloromethyl group in 3-((chloroMethyl)diMethylsilyl)propan-1-ol endows it with the capacity to participate in numerous chemical reactions, making it a valuable reagent for creating diverse organic compounds and intermediates in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 18171-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18171-24:
(7*1)+(6*8)+(5*1)+(4*7)+(3*1)+(2*2)+(1*4)=99
99 % 10 = 9
So 18171-24-9 is a valid CAS Registry Number.
18171-24-9Relevant academic research and scientific papers
Synthesis and conformational analysis of 1,3-azasilinanes
Shainyan, Bagrat A.,Kirpichenko, Svetlana V.,Kleinpeter, Erich
experimental part, p. 7494 - 7501 (2012/09/21)
1-Isopropyl-3-methyl-3-phenyl-1,3-azasilinane 1 and 1-isopropyl-3,3- dimethyl-1,3-azasilinane 2 were synthesized and a detailed analysis of their NMR spectra, conformational equilibria and ring inversion processes is presented. Low temperature 1/sup
Synthesis of L-ascorbic acid derivatives as potential bone remodeling agents taking advantage of the Mitsunobu reaction
Vila?a, Gil,Rubio, Cyril,Susperregui, Jacques,Latxague, Laurent,Déléris, Gérard
, p. 9249 - 9256 (2007/10/03)
The synthesis of ascorbic acid derivatives 7a-d is described. Starting from alkenylacetates 1a-d subjected to a hydrosilylation reaction, the resulting hydroxy chloro silanes 3a-d were obtained in high yield. The latter compounds were reacted with potassium phthalimide followed with hydrazine hydrate to give the amino silanols 5a-d. Ascorbic acid was then alkylated on its 3-hydroxy position to give 7a-d by means of a Mitsunobu reaction.
Benzamide derivatives
-
, (2008/06/13)
Benzamide derivatives of the formula : wherein R1 is optionally substituted alkyl optionally containing double or triple bonds or cycloalkyl rings, which is interrupted by silicon, and optionally interrupted by a hetero atom, and/or by sulphinyl or sulpho
