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Ethyl-pentafluorophenyl-amine is an organic compound with the chemical formula C8H6F5N. It is a derivative of aniline, where one hydrogen atom is replaced by an ethyl group, and four hydrogen atoms are replaced by fluorine atoms. Ethyl-pentafluorophenyl-amine is characterized by its unique electronic properties due to the presence of fluorine atoms, which can significantly influence its reactivity and stability. Ethyl-pentafluorophenyl-amine is used in various chemical reactions and as an intermediate in the synthesis of more complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its structure provides a balance between the electron-donating nature of the ethyl group and the electron-withdrawing effect of the fluorine atoms, making it a versatile building block in organic synthesis.

4070-08-0

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4070-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4070-08-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4070-08:
(6*4)+(5*0)+(4*7)+(3*0)+(2*0)+(1*8)=60
60 % 10 = 0
So 4070-08-0 is a valid CAS Registry Number.

4070-08-0Downstream Products

4070-08-0Relevant academic research and scientific papers

Alkylation of aromatic amines and related compounds using a copper(II)-aluminum(III) couple

Barton, Derek H.R.,Doris, Eric

, p. 3295 - 3298 (1996)

Copper(II)-mediated alkylation of amines and related compounds (e.g. hydrazines, hydrazones, hydroxylamines) using an alkyl aluminum reagent is described. The reaction proceeds selectively and in good yield, utilizing a metal-metal exchange as the key step.

Bis(trialkylsilyl) peroxides as alkylating agents in the copper-catalyzed selective mono-: N -alkylation of primary amides

Sakamoto, Ryu,Sakurai, Shunya,Maruoka, Keiji

supporting information, p. 6484 - 6487 (2017/07/10)

The copper-catalyzed selective mono-N-alkylation of primary amides with bis(trialkylsilyl) peroxides as alkylating agents was reported. The results of a mechanistic study suggest that this reaction should proceed via a free radical process that includes the generation of alkyl radicals from bis(trialkylsilyl) peroxides.

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