2057-47-8 Usage
General Description
4-(1-phenethyl-3-phenyl-propyl)-pyridine is a chemical compound that belongs to the family of pyridine derivatives. It is composed of a pyridine ring with a 4-(1-phenethyl-3-phenyl-propyl) substituent attached to it. 4-(1-PHENETHYL-3-PHENYL-PROPYL)-PYRIDINE is used in research and development for its potential pharmaceutical applications. It may have biological activities such as anti-inflammatory, analgesic, or anti-cancer properties, but further studies are needed to fully understand its potential uses and effects. The specific applications and properties of this compound are still under investigation, and it is not currently used in commercial products.
Check Digit Verification of cas no
The CAS Registry Mumber 2057-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2057-47:
(6*2)+(5*0)+(4*5)+(3*7)+(2*4)+(1*7)=68
68 % 10 = 8
So 2057-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H23N/c1-3-7-19(8-4-1)11-13-21(22-15-17-23-18-16-22)14-12-20-9-5-2-6-10-20/h1-10,15-18,21H,11-14H2
2057-47-8Relevant articles and documents
Potassium Amide-Catalyzed Benzylic C?H Bond Addition of Alkylpyridines to Styrenes
Zhai, Dan-Dan,Zhang, Xiang-Yu,Liu, Yu-Feng,Zheng, Lei,Guan, Bing-Tao
supporting information, p. 1650 - 1653 (2018/01/27)
The benzylic functionalization of alkylpyridines is an important pathway for pyridine derivatives synthesis. The reaction partners, however, were mostly limited to highly reactive polar electrophiles. Herein, we report a potassium amide-catalyzed selective benzylic C?H bond addition of alkylpyridines to styrenes. Potassium bis(trimethylsilyl)amide (KHMDS), a readily available Br?nsted base, showed excellent catalytic activity and chemoselectivity. A series of alkylpyridine derivatives, including benzylic quaternary carbon substituted pyridines, were obtained in good to high yield. Preliminary mechanistic studies revealed that the deprotonation equilibrium is probably responsible for the excellent selectivity.
