39614-78-3 Usage
General Description
6-Ethoxypyridazin-3-amine is a chemical compound with the formula C7H10N4O. It is a derivative of pyridazine and contains an ethoxy group attached to the pyridazine ring. 6-Ethoxypyridazin-3-amine is a weak base and is primarily used in research and pharmaceutical applications. It has potential use in the development of new drugs and pharmaceutical products due to its structural properties and reactivity. 6-Ethoxypyridazin-3-amine may also be used as an intermediate in organic synthesis for the production of various other compounds. Overall, this chemical has potential utility in a range of scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39614-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,1 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39614-78:
(7*3)+(6*9)+(5*6)+(4*1)+(3*4)+(2*7)+(1*8)=143
143 % 10 = 3
So 39614-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3O/c1-2-10-6-4-3-5(7)8-9-6/h3-4H,2H2,1H3,(H2,7,8)
39614-78-3Relevant articles and documents
2-Phenylimidazo[1,2-b]pyridazine derivatives highly active against Haemonchus contortus
Ali, Abdelselam,Cablewski, Teresa,Francis, Craig L.,Ganguly, Ashit K.,Sargent, Roger M.,Sawutz, David G.,Winzenberg, Kevin N.
scheme or table, p. 4160 - 4163 (2011/08/10)
A series of 2-phenylimidazo[1,2-b]pyridazine derivatives were synthesized and evaluated for their in vitro anthelmintic activity against Haemonchus contortus. The most active compounds had in vitro LD99 values of 30 nM, which is comparable to that of the benchmark commercial nematocide, Ivermectin.
A revision of the alcoholysis and alkanethiolysis of 3-amino-6-chloropyridazine
Maes,Lemiere,Dommisse,Haemers
, p. 1215 - 1218 (2007/10/03)
The synthesis of 3-amino-6-alkoxy- and 3-amino-6-alkylthiopyridazines via nucleophilic aromatic substitution on 3-amino-6-chloropyridazine is described. In contrast to literature reports, no pressure tube is required to perform these reactions.
