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2,2,2-Trifluoro-N,N-dimethylethyl-1-amine hydrochloride is a chemical compound with the molecular formula C4H9ClF3N. It is a derivative of 2,2,2-trifluoro-N,N-dimethylethylamine, where the amine group has been protonated to form an ammonium ion. 2,2,2-trifluoro-N,N-dimethylethyl-1-amine hydrochloride is characterized by the presence of three fluorine atoms attached to the same carbon atom, which imparts unique chemical properties due to the electronegativity and small size of fluorine. The hydrochloride salt form indicates that it is a salt derived from the reaction of the parent amine with hydrochloric acid, which is commonly used to increase the solubility and stability of amines in aqueous solutions. 2,2,2-trifluoro-N,N-dimethylethyl-1-amine hydrochloride may be used in various chemical syntheses, particularly in the preparation of pharmaceuticals and agrochemicals, where its unique fluorinated structure can influence the physicochemical properties and biological activity of the final products.

2105-86-4

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2105-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2105-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2105-86:
(6*2)+(5*1)+(4*0)+(3*5)+(2*8)+(1*6)=54
54 % 10 = 4
So 2105-86-4 is a valid CAS Registry Number.

2105-86-4Downstream Products

2105-86-4Relevant academic research and scientific papers

Method for preparing amine compound by reducing amide compound

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Paragraph 0117-0119, (2021/02/10)

The invention relates to a method for preparing an amine compound by reducing an amide compound, which comprises the following steps: in a protective atmosphere, mixing the amide compound or cyclic amide, a zirconium metal catalyst and pinacol borane, carrying out amide reduction reaction at room temperature, and carrying out aftertreatment by using an ether solution of hydrogen chloride after 12-48 hours to obtain an amine hydrochloride compound. The method is simple to operate, low in cost, good in functional group tolerance and wide in substrate range.

Aluminium complex as an efficient catalyst for the chemo-selective reduction of amides to amines

Das, Suman,Karmakar, Himadri,Bhattacharjee, Jayeeta,Panda, Tarun K.

, p. 11978 - 11984 (2019/08/13)

We report an efficient protocol for the catalytic chemo-selective reduction of tert-amides with pinacolborane (HBpin) to afford the corresponding amines in high yields using aluminium complexes [κ2-{Ph2P(X)NC9H6N}Al(Me)2] [X = S (2a), Se (2b)] as pre-catalysts at room temperature. The aluminium complexes were prepared from the reaction of [Ph2P(X)NC9H6N] [X = S (1a), Se (1b)] and trimethylaluminium in toluene. The solid-state structure of complex 2b is established. Tertiary amides with a wide array of electron-withdrawing and electron-donating functional groups were easily converted to the desired products through the selective cleavage of the amides' CO bond by aluminium hydride as an active species. A kinetic study of the catalytic reaction is also reported.

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