149021-01-2 Usage
Description
(Trimethylsilyldifluoromethyl)benzene, with the chemical formula C10H14F2Si, is a colorless liquid at room temperature. It is a significant chemical compound utilized as a building block in organic synthesis, particularly known for its ability to introduce difluoromethyl groups into organic molecules. This characteristic makes it a valuable tool in the development of new materials and drugs.
Uses
Used in Pharmaceutical Industry:
(Trimethylsilyldifluoromethyl)benzene is used as a reagent for the production of various pharmaceuticals. Its ability to introduce difluoromethyl groups into organic molecules aids in the synthesis of new drugs, potentially enhancing their efficacy and properties.
Used in Agrochemical Industry:
In the agrochemical industry, (Trimethylsilyldifluoromethyl)benzene serves as a reagent in the manufacturing process of various agrochemicals. Its role in introducing difluoromethyl groups can lead to the development of more effective and targeted agrochemical products.
Used in Electronic Materials Manufacturing:
(Trimethylsilyldifluoromethyl)benzene is also utilized in the production of electronic materials. Its unique properties contribute to the creation of advanced materials with specific characteristics required for various applications in the electronics sector.
Safety Note:
It is crucial to handle (Trimethylsilyldifluoromethyl)benzene with care due to its volatile nature. Proper safety measures should be taken to prevent potential hazards associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 149021-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,0,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 149021-01:
(8*1)+(7*4)+(6*9)+(5*0)+(4*2)+(3*1)+(2*0)+(1*1)=102
102 % 10 = 2
So 149021-01-2 is a valid CAS Registry Number.
149021-01-2Relevant articles and documents
Selective electrochemical synthesis and reactivity of functional benzylic fluorosilylsynthons
Clavel, Philippe,Lessene, Guillaume,Biran, Claude,Bordeau, Michel,Roques, Nicolas,Trévin, Stéphane,Montauzon, Dominique De
, p. 301 - 310 (2001)
Electrochemical reductive silylation of meta-(trifluoromethyl)arenes by the sacrificial anode technique selectively led to meta-trimethylsilyldifluoromethylarenes (ArCF2TMS), in the presence of an excess of TMSCl and in a THF/cosolvent mixture
Cu-deposits on Mg metal surfaces promote electron transfer reactions
Utsumi, Shinya,Katagiri, Toshimasa,Uneyama, Kenji
, p. 1085 - 1091 (2012/03/07)
The enhancement of the electron transfer processes in the Grignard reagent formation-type ring silylation and the defluorination-silylation of perfluoroalkyl benzenes by Cu(0)-deposited Mg metal were confirmed. Microscopic analysis and substituent effects implied a different reduction process in the presence of Cu-deposited Mg metal than in the presence of bare Mg metal.
Selective electrosynthesis of (trimethylsilyldifluoro)methylbenzene, a PhCF2-precursor; conditions for a molar scale preparation without HMPA
Clavel,Léger-Lambert,Biran,Serein-Spirau,Bordeau,Roques,Marzouk
, p. 829 - 834 (2007/10/03)
Electrochemical reductive silylation of trifluoromethylbenzene by the sacrificial anode technique selectively led, in a THF/DMPU mixture instead of THF/HMPA and according to the charge passed, to the corresponding mono-, bis- or tris-trimethylsilyl derivatives, respectively PhCF2TMS, PhCF(TMS)2 and PhC(TMS)3. This reaction, without any chemical equivalent, was extended to a molar scale synthesis, using a tubular flow cell.
