385435-07-4 Usage
Chemical structure
2(1H)-Pyridinone derivative with an ethoxy group at position 4 and a phenyl group at position 6
Biological activities
Antiviral, antibacterial, antifungal, and antitumor properties
Potential applications
Treatment of neurodegenerative disorders
Stereochemistry
6S
Importance of stereochemistry
The 6S stereochemistry is important for the compound's activity
Preclinical studies
Research has shown promising results in preclinical studies
Industry interest
Ongoing research in the pharmaceutical industry for potential therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 385435-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,5,4,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 385435-07:
(8*3)+(7*8)+(6*5)+(5*4)+(4*3)+(3*5)+(2*0)+(1*7)=164
164 % 10 = 4
So 385435-07-4 is a valid CAS Registry Number.
385435-07-4Relevant articles and documents
Addition of dienolates to sulfinimines. Stereoselective synthesis of dihydropyridones
Kaw, Robert
, p. 8385 - 8390 (2007/10/03)
The vinylogous Mannich reaction of sulfinimines with dienolates was investigated. Lithium and trimethylsilyl enolates of ethyl 3-ethoxycrotonate reacted with enantiopure 10-isobornylsulfinimines to give derivatives of δ-aminoacids which were cyclised to 6-aryl substituted derivatives of 2(1H)-pyridinones. 6-Aryl substituted 2,4-piperidinediones with either (S) or (R) configuration were analogously obtained using lithium and TMS enolates of 2,2,6-trimethyl-1,3-dioxin-4-one.
