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α-Isopropyl-β-phenylpropionitrile, also known as 3-phenyl-2-methylpropanenitrile, is an organic compound with the chemical formula C??H??N. It is a colorless liquid with a molecular weight of 147.20 g/mol. α-isopropyl-β-phenylpropionitrile is characterized by the presence of an isopropyl group (CH?-CH(CH?)), a phenyl group (C?H?), and a nitrile group (CN). It is synthesized through various methods, such as the reaction of benzyl chloride with potassium cyanide or the condensation of acetone with benzyl cyanide. α-Isopropyl-β-phenylpropionitrile is used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential use as a precursor in the synthesis of certain drugs and as a building block in the creation of complex organic molecules.

53244-15-8

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53244-15-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53244-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53244-15:
(7*5)+(6*3)+(5*2)+(4*4)+(3*4)+(2*1)+(1*5)=98
98 % 10 = 8
So 53244-15-8 is a valid CAS Registry Number.

53244-15-8Downstream Products

53244-15-8Relevant articles and documents

Preparation of 2-arylquinolines from β-arylpropionitriles with aryllithiums and NIS through iminyl radical-mediated cyclization

Naruto, Hiroki,Togo, Hideo

, p. 5760 - 5770 (2019)

Treatment of β-arylpropionitriles with aryllithiums, followed by the reaction with water and then with NIS under irradiation with a tungsten lamp gave 2-arylquinolines in good to moderate yields. The present reaction proceeds through the formation of N-iodoimines from imines with NIS, the generation of imino-nitrogen-centered radicals, and their cyclization onto the aromatic rings of the imines to form 2-aryl-3,4-dihydroquinolines. Finally, the oxidation of 2-aryl-3,4-dihydroquinolines with NIS proceeds smoothly to generate 2-arylquinolines.

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