87544-92-1 Usage
Chemical compound
2-[(4-oxo-3,4-dihydropyrido[3,4-d]pyridazin-1-yl)amino]ethyl acetate
Structure
Acetate ester derivative of an aminoethyl group with a pyridazine ring containing a ketone and an amino group
Potential pharmaceutical applications
Interacts with biological systems, potential treatment for certain diseases or conditions
Handling
Caution required, follow proper safety protocols
Unknown effects
Not fully understood, further research and testing needed to determine applications and risks
Check Digit Verification of cas no
The CAS Registry Mumber 87544-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,4 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87544-92:
(7*8)+(6*7)+(5*5)+(4*4)+(3*4)+(2*9)+(1*2)=171
171 % 10 = 1
So 87544-92-1 is a valid CAS Registry Number.
87544-92-1Relevant articles and documents
PYRIDAZINES CONDENSED WITH A HETERO RING, II. PYRIDO AMINOPYRIDAZINES, I. SEPARATION AND STRUCTURE DETERMINATION OF THE ISOMERIC MONOCHLORO COMPOUNDS OBTAINED BY HYDROLYSIS OF 1,4-DICHLOROPYRIDOPYRIDAZINE
Koermendy, K.,Kovacs, T.,Ruff, F.,Koevesdi, I.
, p. 487 - 500 (2007/10/02)
The separation of the mixture of isomers 2 and 3, obtained by hydrolysis of 1,4-dichloropyrido pyridazine, was accomplished and the structures of the isomers (2: 1-Cl; 3:4-Cl) were verified by synthesis.Aminolysis of 2 and 3 yielded the hydroxy-ethylamino derivatives 4 and 5; a mixture of these compounds can also be synthesized from 2-tosyloxyethylcinchomeronic imide (20 -> 4, 5) in a good yield (84percent).