2057-47-8 Usage
Description
4-(1-PHENETHYL-3-PHENYL-PROPYL)-PYRIDINE is a pyridine derivative chemical compound characterized by a pyridine ring with a 4-(1-phenethyl-3-phenyl-propyl) substituent. It is currently in the research and development phase for potential pharmaceutical applications due to its possible biological activities.
Uses
Used in Pharmaceutical Research and Development:
4-(1-PHENETHYL-3-PHENYL-PROPYL)-PYRIDINE is used as a compound under investigation for its potential biological activities, such as anti-inflammatory, analgesic, or anti-cancer properties. 4-(1-PHENETHYL-3-PHENYL-PROPYL)-PYRIDINE's specific applications and properties are still being explored, and it is not yet utilized in commercial products. Further studies are required to fully understand its potential uses and effects in the pharmaceutical industry.
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.
