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Cyclohexanamine lithium, also known as lithium cyclohexylamine or lithium hexahydrobenzylamine, is a chemical compound with the formula C6H13NLi. It is a colorless, hygroscopic solid that is soluble in water and organic solvents. cyclohexanamine lithium is derived from cyclohexylamine, a cyclic amine, and lithium, a highly reactive alkali metal. Cyclohexanamine lithium is primarily used as a strong base and a nucleophile in various organic synthesis reactions, such as the formation of amines, amides, and other nitrogen-containing compounds. Due to its reactivity, it is essential to handle cyclohexanamine lithium with care, typically under an inert atmosphere or in a controlled environment.

4819-94-7

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4819-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4819-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4819-94:
(6*4)+(5*8)+(4*1)+(3*9)+(2*9)+(1*4)=117
117 % 10 = 7
So 4819-94-7 is a valid CAS Registry Number.

4819-94-7Upstream product

4819-94-7Relevant academic research and scientific papers

Alkyl-ended ansa-bis(amidinate) ligands from aliphatic primary amines and multinuclear lithium derivatives

Bai, Sheng-Di,Liu, Rui-Qin,Guan, Fei,Wang, Tao,Tong, Hong-Bo,Guo, Jian-Ping,Liu, Dian-Sheng

, p. 265 - 267 (2013)

A practical synthetic pathway to alkyl-ended ansa-bis(amidinate) ligands was developed via linking the freshly prepared aliphatic group substituted lithium amidinate and the subsequent deprotonation. The lithium complexes prepared by this method were char

Kinetic acidities of some hydrocarbons by tritium NMR

Streitwieser, Andrew,Linfeng, Xie,Speers, Peter,Williams, Philip G.

, p. S209-S211 (2007/10/03)

Exchange rates in cyclohexylamine-N-3H catalyzed by cesium cyclohexylamide were determined by 3H NMR for the vinyl positions of 3,3-dimethyl-1-butene (1-trans > 1-cis > 2-) and the cyclopropyl methylene positions of norcarane (exo >

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