10074-42-7 Usage
Description
Lithium, cyclohexyl-, also known as lithium cyclohexylacetic acid, is a chemical compound that serves as a lithium salt of cyclohexylacetic acid. It is a versatile building block for the synthesis of various pharmaceuticals and has been utilized as a reagent in organic synthesis. Additionally, it has applications in the treatment of certain mental health conditions and in the manufacturing of lithium-ion batteries and other industrial applications. Despite its potential side effects, such as gastrointestinal and skin irritation, lithium, cyclohexylholds significant value in both pharmaceutical and industrial sectors.
Uses
Used in Pharmaceutical Industry:
Lithium, cyclohexylis used as a building block for the synthesis of various pharmaceuticals due to its unique chemical properties and reactivity.
Used in Organic Synthesis:
Lithium, cyclohexylis used as a reagent in organic synthesis, facilitating the formation of new compounds and contributing to the development of novel drugs and materials.
Used in Mental Health Treatment:
Lithium, cyclohexylis used as a therapeutic agent in the treatment of certain mental health conditions, providing relief and management of symptoms.
Used in Lithium-Ion Battery Manufacturing:
Lithium, cyclohexylis used in the manufacturing of lithium-ion batteries, contributing to the development of energy storage solutions for various applications.
Used in Industrial Applications:
Lithium, cyclohexylis employed in various industrial applications, leveraging its chemical properties for diverse uses in different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 10074-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10074-42:
(7*1)+(6*0)+(5*0)+(4*7)+(3*4)+(2*4)+(1*2)=57
57 % 10 = 7
So 10074-42-7 is a valid CAS Registry Number.
10074-42-7Relevant articles and documents
Hydrometalation of fluoroallenes
Kuehnel, Moritz F.,Lentz, Dieter
, p. 4747 - 4755 (2009)
Tetrafluoroallene (1) and 1,1-difluoroallene (2) react under mild conditions with group 6 and 7 transition metal hydride complexes Cp(CO) 3MoH (4), CO5MnH (5), Cp2WH2 (9), and Cp2MoH2 (10)
Alkali metal-containing, organometallic products
-
, (2008/06/13)
An alkali metal-containing, organometallic product, which is hydrocarbon-soluble, is prepared by reacting an organo-alkali metal reactant in which the alkali metal atom is bonded to a carbon atom, e.g. cyclohexyl-lithium, with a di(organooxy)-alkaline earth metal reactant, e.g. di-n-butoxy-magnesium, in an organic solvent at about -20° to +120°C. The organo-alkali metal reactant can be prepared by reacting an organo halide with an alkali metal, and this can be done in situ, i.e. in the presence of the di(organooxy)-alkaline earth metal reactant. The organometallic product has approximately the same chemical reactivity as the organo-alkali metal reactant from which it is prepared, but is more soluble in hydrocarbon solvents.
