125444-10-2 Usage
Uses
Used in Organic Synthesis:
Lithium, [2,4,6-tris[bis(trimethylsilyl)methyl]phenyl]is used as a reagent in organic synthesis for its strong basic and reducing properties, which facilitate the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Metallation of Aromatic Compounds:
In the field of organic chemistry, lithium TMP is used as a metallating agent for aromatic compounds, allowing for the introduction of metal groups and enhancing the reactivity of these compounds for further reactions.
Used in Pharmaceutical Production:
Lithium, [2,4,6-tris[bis(trimethylsilyl)methyl]phenyl]is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, lithium TMP is employed in the synthesis of agrochemicals, aiding in the production of pesticides, herbicides, and other agricultural products.
Used in Energy Storage Applications:
Lithium, [2,4,6-tris[bis(trimethylsilyl)methyl]phenyl]is used as a component in lithium-ion batteries and other advanced materials for energy storage, capitalizing on its highly reactive nature and high lithium content to improve the performance and efficiency of these technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 125444-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,4 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125444-10:
(8*1)+(7*2)+(6*5)+(5*4)+(4*4)+(3*4)+(2*1)+(1*0)=102
102 % 10 = 2
So 125444-10-2 is a valid CAS Registry Number.
125444-10-2Relevant articles and documents
Synthesis of an acyclic diselenodithioether ligand tethered with bulky substituents and its application to the synthesis of a distorted octahedral palladium(II) complex
Takeda, Nobuhiro,Isobe, Toru,Tokitoh, Norihiro
, p. 549 - 556 (2007)
A new o-phenylene-bridged diselenodithioether ligand tethered with an extremely bulky substituent, 2,4,6-tris[bis(trimethylsilyl)methyljphenyl (Tbt) group, at both terminal selenium atoms, [TbtSe(o-phenylene)S] 2(o-phenylene) (3), was synthesiz
