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α-Benzoyl-α-(2-naphthyl) acetonitrile is an organic compound with the chemical formula C18H13NO. It is a derivative of acetonitrile, featuring a benzoyl group (C6H5CO) attached to the α-carbon and a 2-naphthyl group (C10H7) attached to the same carbon. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It is a white crystalline solid that is soluble in organic solvents. The compound is often used as an intermediate in the preparation of other more complex molecules, highlighting its importance in the field of organic chemistry.

51074-13-6

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51074-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51074-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51074-13:
(7*5)+(6*1)+(5*0)+(4*7)+(3*4)+(2*1)+(1*3)=86
86 % 10 = 6
So 51074-13-6 is a valid CAS Registry Number.

51074-13-6Downstream Products

51074-13-6Relevant articles and documents

Asymmetric Transfer Hydrogenation of α-Substituted-β-Keto Carbonitriles via Dynamic Kinetic Resolution

Wang, Fangyuan,Yang, Tilong,Wu, Ting,Zheng, Long-Sheng,Yin, Congcong,Shi, Yongjie,Ye, Xiang-Yu,Chen, Gen-Qiang,Zhang, Xumu

supporting information, p. 2477 - 2483 (2021/02/16)

A catalytic protocol for the enantio- and diastereoselective reduction of α-substituted-β-keto carbonitriles is described. The reaction involves a DKR-ATH process with the simultaneous construction of β-hydroxy carbonitrile scaffolds with two contiguous stereogenic centers. A wide range of α-substituted-β-keto carbonitriles were obtained in high yields (94%-98%) and excellent enantio- and diastereoselectivities (up to >99% ee, up to >99:1 dr). The origin of the diastereoselectivity was also rationalized by DFT calculations. Furthermore, this methodology offers rapid access to the pharmaceutical intermediates of Ipenoxazone and Tapentadol.

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