18182-40-6 Usage
Description
((CH3)2NCH2Si(CH3)3), also known as dimethylaminomethyl(trimethylsilyl) silane, is a chemical compound characterized by a silicon atom bonded to three methyl groups and a dimethylaminomethyl group. It is recognized for its versatile reactivity and significant role in various chemical and industrial processes.
Usage:
Used in Organic Synthesis:
((CH3)2NCH2Si(CH3)3) is used as a reagent for the protection of hydroxyl groups in alcohols and phenols, which is crucial in organic synthesis to prevent unwanted reactions at the hydroxyl functional groups.
Used in Organosilicon Chemistry:
((CH3)2NCH2Si(CH3)3) is used as a precursor in organosilicon chemistry, a field that involves the study and application of silicon-containing compounds.
Used in Catalyst Stabilization:
((CH3)2NCH2Si(CH3)3) is used as a stabilizer for certain metal catalysts, enhancing their performance and longevity in various chemical reactions.
Used in Pharmaceutical Production:
((CH3)2NCH2Si(CH3)3) is utilized in the production of pharmaceuticals, contributing to the synthesis of various drugs and medicinal compounds.
Used in Materials Science:
((CH3)2NCH2Si(CH3)3) is employed in the field of materials science, where it aids in the development of new materials with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 18182-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18182-40:
(7*1)+(6*8)+(5*1)+(4*8)+(3*2)+(2*4)+(1*0)=106
106 % 10 = 6
So 18182-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H17NSi/c1-7(2)6-8(3,4)5/h6H2,1-5H3
18182-40-6Relevant articles and documents
Anionic rearrangement of the germyl and silyl groups in dimethylammonium N-methylide and related compounds
Inoue, Sumie,Urayama, Shin'ichi,Sugiura, Hiroyo,Sato, Yoshiro
, p. 25 - 30 (2007/10/02)
The reaction of - and trimethylammonium iodides (3a and 3c) with n-butyllithium gives N-- and N-dimethylamines (5a and 5b), respectively.A mixture of 5a and 5b is obtained from the reaction of trimethylammonium iodide (3b).Use of lithium diisopropylamide in place of n-butyllithium gives the corresponding 1,1-bis(trimethylelemento)ethylenes (8a, 8b, and 8c) as the main products.
Ylide Reactions of Benzyldimethylammonium Halides
Sato, Yoshiro,Yagi, Yoko,Koto, Masami
, p. 613 - 617 (2007/10/02)
Deprotonation of benzyldimethylammonium halides (10) with sodium amide or n-butyllithium afforded silylated ylide intermediates 11, which were rearranged into N,N-dimethyl-2-benzylamines (13) accompanied by the formation of Sommelet-Hauser and Stevens rearrangement products (12 and 22).The ylide formation by the cleavage of carbon-silicon bonds also is discussed in the reaction of 10 with sodium amide and lithium aluminum hydride.