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(2,2-difluoropropyl)-phenyl-amine is an organic compound with the molecular formula C9H10F2N. It is a derivative of phenylamine, featuring a 2,2-difluoropropyl group attached to the nitrogen atom. (2,2-difluoropropyl)-phenyl-amine is characterized by its fluorinated alkyl chain, which can influence its physical and chemical properties, such as reactivity, solubility, and boiling point. It is a colorless liquid with a molecular weight of 175.18 g/mol. The compound may be used in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and potential reactivity. It is important to handle (2,2-difluoropropyl)-phenyl-amine with care, as it may have specific safety and environmental considerations due to its amine functionality and fluorinated components.

7594-18-5

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7594-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7594-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7594-18:
(6*7)+(5*5)+(4*9)+(3*4)+(2*1)+(1*8)=125
125 % 10 = 5
So 7594-18-5 is a valid CAS Registry Number.

7594-18-5Relevant academic research and scientific papers

gem-difluorination of aminoalkynes via highly reactive dicationic species in superacid HF-SbF5: Application to the efficient synthesis of difluorinated cinchona alkaloid derivatives

Cantet, Anne-Celine,Carreyre, Helene,Gesson, Jean-Pierre,Jouannetaud, Marie-Paule,Renoux, Brigitte

, p. 2875 - 2878 (2008/09/19)

(Chemical Equation Presented) A variety of alkynylated amines, amides, and imides are reacted in the superacid system HF-SbF5 to give regioselectively new β-gem-difluoroamines. The reaction, which is not observed in pure HF, is consistent with

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