10074-42-7

Basic information

• Product Name: Lithium, cyclohexyl-
• CAS NO: 10074-42-7
• Molecular Formula: C6H11Li
• Molecular Weight: 90.0943
• Mol File: 10074-42-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Lithium, cyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Lithium, cyclohexyl-(10074-42-7)
• EPA Substance Registry System: Lithium, cyclohexyl-(10074-42-7)

Safety Data

• Hazardous Substances Data: 10074-42-7(Hazardous Substances Data)

Usage

General Description

Lithium cyclohexyl is a chemical compound that is used in the production of pharmaceuticals. It is a lithium salt of cyclohexylacetic acid, a common building block for drugs. Lithium, cyclohexyl- has been used as a reagent in organic synthesis as well as in the treatment of some mental health conditions. It is also used in the manufacturing of lithium-ion batteries and other industrial applications. Lithium cyclohexyl is known for its potential side effects which can include gastrointestinal irritation and skin irritation. Overall, this compound has various uses in the pharmaceutical and industrial sectors.

Upstream product

• 542-18-7 cyclohexyl chloride 
• 7439-93-2 lithium 

Downstream Products

• 6476-37-5 dicyclohexylphenylphosphine 
• 74046-22-3 (+)-Armepavine methochloride 
• 77970-98-0 (Z)-4-Cyclohexyl-2-methyl-but-2-en-1-ol 
• 77971-02-9 (E)-4-Cyclohexyl-2-methyl-but-2-en-1-ol 
• 823-76-7 Cyclohexyl methyl ketone 
• 74810-77-8 bis(dimethylamino)cyclohexylphosphine 
• 133157-77-4 (3S,7R,8aR)-3-tert-Butyl-7-cyclohexyl-7-methyl-tetrahydro-oxazolo[2,3-b][1,3]oxazin-5-one 
• 135033-59-9 (S)-Cyclohexyl-phenyl-(3R,7aS)-tetrahydro-pyrrolo[1,2-c]oxazol-3-yl-methanol 
• 263720-75-8 1-cyclohexyl-3-triisopropylsilanyl-prop-2-yn-1-ol 
• 591-51-5 phenyllithium 
• 2786-01-8 (4-trifluoromethylphenyl)lithium 
• 199612-37-8 [(Me₃SiNCH₂CH₂)3N]Mo(cyclohexyl) 
• 3712-40-1 tert-butyl cyclohexylcarbamate 
• 76814-99-8 chloro(cyclohexyl)diphenylsilane 

Relevant articles and documents

Hydrometalation of fluoroallenes

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

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.