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1-Adamantyllithium, also known as 1-Lithioadamantane, is an organolithium compound with the chemical formula C10H15Li. It is a colorless, highly reactive, and moisture-sensitive solid, often used as a strong base and nucleophile in organic synthesis. Derived from the adamantane molecule, 1-Adamantyllithium exhibits unique steric properties due to its rigid, cage-like structure, which influences its reactivity and selectivity in various chemical reactions. 1-Adamantyllithium is commonly prepared by the reaction of adamantane with lithium metal or n-butyllithium and is employed in the synthesis of various organic compounds, including pharmaceuticals and natural products. Due to its sensitivity to air and moisture, it must be handled under an inert atmosphere, such as nitrogen or argon, and stored away from light and heat.

3732-30-7

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3732-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3732-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3732-30:
(6*3)+(5*7)+(4*3)+(3*2)+(2*3)+(1*0)=77
77 % 10 = 7
So 3732-30-7 is a valid CAS Registry Number.

3732-30-7Upstream product

3732-30-7Relevant 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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