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N-(2,2-difluoroethyl)aniline is an organic compound with the chemical formula C8H8F2N. It is a derivative of aniline, where one hydrogen atom on the nitrogen atom is replaced by a 2,2-difluoroethyl group. N-(2,2-difluoroethyl)aniline is a colorless liquid with a density of 1.15 g/cm3 and a boiling point of 195-197°C. It is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. N-(2,2-difluoroethyl)aniline is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications in the chemical industry, it is essential to handle N-(2,2-difluoroethyl)aniline with care, as it may have toxic effects on human health and the environment.

405-17-4

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405-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 405-17-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 405-17:
(5*4)+(4*0)+(3*5)+(2*1)+(1*7)=44
44 % 10 = 4
So 405-17-4 is a valid CAS Registry Number.

405-17-4Relevant academic research and scientific papers

Photoredox-Catalyzed Defluorinative Functionalizations of Polyfluorinated Aliphatic Amides and Esters

Ye, Jian-Heng,Bellotti, Peter,Heusel, Corinna,Glorius, Frank

, (2022/01/20)

Selective C?F bond functionalization of perfluoalkyl units has huge potential towards accessing functionalized organofluorinated compounds, but remains challenging due to the high C?F bond strength and inherent selectivity challenges. We report a new catalytic approach to the selective functionalization of strong C?F bonds in polyfluorinated aliphatic esters and amides. This simple reaction proceeds in mild and operational fashion with divergent conversions, including hydrodefluorination, defluoroalkylation, and defluoroalkenylation, affording a diverse array of important partially fluorinated motifs. Straightforward downstream chemistry towards fluorinated alcohols, amines and drug derivatives highlights the potential of the protocol.

Direct N-Alkylation/Fluoroalkylation of Amines Using Carboxylic Acids via Transition-Metal-Free Catalysis

Lu, Chunlei,Qiu, Zetian,Xuan, Maojie,Huang, Yan,Lou, Yongjia,Zhu, Yiling,Shen, Hao,Lin, Bo-Lin

supporting information, p. 4151 - 4158 (2020/08/21)

A scalable protocol of direct N-mono/di-alkyl/fluoroalkylation of primary/secondary amines has been constructed with various carboxylic acids as coupling agents under the catalysis of a simple air-tolerant inorganic salt, K3PO4. Advantageous features include 100 examples, 10 drugs and drug-like amines, fluorinated complex tertiary amines, gram-scale synthesis and isotope-labelling amine, thus demonstrating the potential applicability in industry of this methodology. The involvement of relatively less reactive silicon-hydride compared with the traditional reactive metal-hydride or boron-hydride species required to reduce the amide intermediates presumably contributes to the remarkable functional group compatibility. (Figure presented.).

Cu-Catalyzed/mediated synthesis of N-fluoroalkylanilines from arylboronic acids: fluorine effect on the reactivity of fluoroalkylamines

Wang, Hui,Tu, Yuan-Hong,Liu, De-Yong,Hu, Xiang-Guo

supporting information, p. 6634 - 6637 (2018/09/29)

An oxidative coupling reaction of fluoroalkylamines with arylboronic acids has been achieved for the first time. Fluorine has profound influence on the reactivity and fluoroalkylated amines have the following reactivity trend: difluoroethylamine > trifluo

Electrolytic Reactions of Fluoroorganic Compounds. 14. Regioselective Anodic Methoxylation of N-(Fluoroethyl)amines. Preparation of Highly Useful Fluoroalkylated Building Blocks

Fuchigami, Toshio,Ichikawa,, Shinji

, p. 607 - 615 (2007/10/02)

Anodic methoxylation of various types of N-(fluoroethyl)amines, ArRNCH2Rf (Rf = CF3, CHF2, CH2F, etc.) has been systematically studied and it was found that a methoxy group was exclusively or preferentially introduced into the position α to the fluoromethyl (Rf) group, depending on the Rf and R groups.The effect of the Rf group on the promotion of the anodic α-methoxylation decreased in the order CF3, CHF2, and CH2F.This remarkable promotion effect and unique regioselectivity can be explained mainly in terms of the α-CH kinetic acidities of the cation radicals formed by one-electron oxidation of the amines.The α-methoxylated products are highly useful precursors for the construction of carbon-carbon bonds α to the trifluoromethyl and difluoromethyl groups, which is difficult by other methods.

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