1017601-66-9 Usage
General Description
1-BENZYL-5-(3-HYDROXYPHENYL)-2,3-DIHYDRO-4-PYRIDINONE, also known as BPN, is a synthetic chemical compound that belongs to the class of pyridinones. It is characterized by a benzyl group attached to the nitrogen of the pyridinone ring, as well as a hydroxyphenyl group at the 5-position. BPN has been studied for its potential pharmacological activities, including its ability to modulate the activity of enzymes such as p60v-src and protein kinases. It has also been investigated for its potential neuroprotective and antioxidant properties. Additionally, BPN has been used as a precursor in the synthesis of various pharmaceutical compounds. Overall, 1-BENZYL-5-(3-HYDROXYPHENYL)-2,3-DIHYDRO-4-PYRIDINONE has shown promise in various medicinal and chemical applications due to its unique structure and potential bioactivities.
Check Digit Verification of cas no
The CAS Registry Mumber 1017601-66-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,6,0 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1017601-66:
(9*1)+(8*0)+(7*1)+(6*7)+(5*6)+(4*0)+(3*1)+(2*6)+(1*6)=109
109 % 10 = 9
So 1017601-66-9 is a valid CAS Registry Number.
1017601-66-9Relevant articles and documents
Palladium(II)-catalyzed direct arylation of enaminones using organotrifluoroborates
Ge, Haibo,Niphakis, Micah J.,Georg, Gunda I.
, p. 3708 - 3709 (2008/09/21)
A Pd(II)-catalyzed reaction for the direct arylation of cyclic enaminones is reported. The reactivity of electron-rich, electron-poor, and sterically encumbered organotrifluoroborates was investigated. This reaction represents a unique use for organotrifluoroborates as coupling partners and discloses the utility of enaminones for direct-functionalization reactions. It provides immediate access to arylpiperidine, indolizidine, and quinolizidine scaffolds from the corresponding mono- and bicyclic, unattenuated enaminones. Copyright