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Trimethyl-3,5,7 adamantyl-1 lithium is a complex organic compound with the molecular formula C13H21Li. It is derived from the adamantane structure, which is a highly stable and rigid hydrocarbon consisting of four fused cyclohexane rings. In trimethyl-3,5,7 adamantyl-1 lithium, three methyl groups (CH3) are attached to the adamantane core, and a lithium atom is bonded to the 1-position carbon atom. This lithium-containing compound is of interest in organic synthesis, particularly in the formation of organolithium reagents, which are useful intermediates in various chemical reactions. The presence of the lithium atom makes it a strong base and a nucleophile, allowing it to participate in a range of organic transformations, such as coupling reactions and the formation of carbon-carbon bonds.

86550-18-7

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86550-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86550-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,5 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86550-18:
(7*8)+(6*6)+(5*5)+(4*5)+(3*0)+(2*1)+(1*8)=147
147 % 10 = 7
So 86550-18-7 is a valid CAS Registry Number.

86550-18-7Relevant academic research and scientific papers

High-Yield Direct Synthesis of a New Class of Tertiary Organolithium Derivatives of Polycyclic Hydrocarbons

Molle, G.,Bauer, P.,Dubois, J. E.

, p. 2975 - 2981 (2007/10/02)

For the first time, 1- and 2-adamantyllithium, 1-diamantyllithium, 3,5,7-trimethyl-1-adamantyllithium, 1-twistyllithium, 3-methyl-7-noradamantyllithium, 1-triptycyllithium, and 3-homoadamantyllithium have been directly synthesized from the reaction of an organic halide and lithium metal.By use of certain experimental parameters, the phenomena at the metal-solution interface are controlled, thereby resulting in exceptionally high yields of this new class of organometallic compounds (>75percent, except in the case of 3-homoadamantyllithium).Competition between formation of the organometallic compound and formation of solvent-attack byproducts is determined by the degree of adsorption of the transient species (anion radical RX-. or radical pair R..Li) generated at the metal surface during attack by the halogenated derivative.

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