82616-41-9 Usage
Type
Naphthyridine derivative
Structural Features
Two benzyl groups attached
One hydroxy group
One methyl group
Ring Structure
Naphthyridine ring
Known as
1,6-dialkyl-2-hydroxy-7-methyl-1,6-naphthyridine-4,5(1H,6H)-dione
Potential Applications
Medicinal chemistry
Biological Activities
Exhibits anti-inflammatory properties
Acts as an anticoagulant
Cancer Research
Shows promising results in inhibiting the growth of certain cancer cell lines
Further Research
Required to fully understand its biological activities and potential therapeutic uses
Check Digit Verification of cas no
The CAS Registry Mumber 82616-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82616-41:
(7*8)+(6*2)+(5*6)+(4*1)+(3*6)+(2*4)+(1*1)=129
129 % 10 = 9
So 82616-41-9 is a valid CAS Registry Number.
82616-41-9Relevant articles and documents
REACTION OF ETHYL β-ALKYLAMINOCROTONATES IN THE PRESENCE OF ORGANIC ACID
Yamato, Masatoshi,Sato, Koichi,Hashigaki, Kuniko,Ninomiya, Mayumi
, p. 1263 - 1268 (2007/10/02)
Condensation of ethyl β-alkylaminocrotonates, obtained from ethyl acetoacetate and amines, in the presence of 3-mercaptopropionic acid gave 1,6-naphthyridine-2,5-dione derivatives.The structures of these compounds were determined on the basis of several i
