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N-(2-adamantyl)benzylideneamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24199-58-4

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24199-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24199-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24199-58:
(7*2)+(6*4)+(5*1)+(4*9)+(3*9)+(2*5)+(1*8)=124
124 % 10 = 4
So 24199-58-4 is a valid CAS Registry Number.

24199-58-4Relevant academic research and scientific papers

1-ADAMANTYLAZETIDIN-2-ONE DERIVATIVES AND DRUGS CONTAINING SAME

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Page/Page column 14, (2010/04/23)

It is to provide a novel compound useful for preventing and/or treating diseases that involves 11β-hydroxysteroid dehydrogenase 1, particularly diabetes, insulin resistance, diabetes complication, obesity, dyslipidemia, hypertension, fatty liver, or metab

Copper-nitrene complexes in catalytic C-H amination

Badiei, Yosra M.,Dinescu, Adriana,Dai, Xuliang,Palomino, Robert M.,Heinemann, Frank W.,Cundari, Thomas R.,Warren, Timothy H.

supporting information; experimental part, p. 9961 - 9964 (2009/05/07)

(Chemical Equation Presented) Hydrocarbons activate! Isolable β-diketiminato dicopper-nitrene complexes such as 1 derived from the reaction of [{(Cl2NN)Cu}2(μ-benzene)] and 1-adamantylazide are potent towards nitrene insertion into unactivated sp 3-hybridized C-H bonds. 1 allows stoichiometric and catalytic intermolecular C-H amination of hydrocarbons to give secondary amines (see scheme). Catalyst loadings as low as 0.05 mol% may be used.

SYNTHESIS AND TRANSFORMATIONS OF N-ADAMANTYL-SUBSTITUTED OXAZIRIDINES

Isaev, S. D.,Novoselov, E. F.,Yurchenko, A. G.

, p. 103 - 108 (2007/10/02)

N-Adamantyl-substituted oxaziridines were obtained by the oxidation of the Schiff bases synthesized from adamantyl-containing amines with peroxyacetic acid.The thermal rearrangement and fragmentation under the influence of Fe(II) ions, leading to nitrones

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