64068-10-6 Usage
Uses
Used in Pharmaceutical Industry:
(6-chloro-7-methylimidazo[1,2-b]pyridazin-2-yl)acetic acid is used as a building block for the synthesis of pharmaceutical drugs due to its unique chemical structure and potential pharmaceutical properties. Its ability to inhibit certain enzymes and receptors makes it a valuable compound in the development of new medications.
Used in Drug Discovery:
In the field of drug discovery, (6-chloro-7-methylimidazo[1,2-b]pyridazin-2-yl)acetic acid is used as a starting point for the development of new therapeutic agents. Its potential anti-cancer and anti-inflammatory activities make it an attractive candidate for further research and development, with the aim of creating novel treatments for various diseases and conditions.
Used in Medicinal Chemistry Research:
(6-chloro-7-methylimidazo[1,2-b]pyridazin-2-yl)acetic acid is employed as a subject of study in medicinal chemistry research. Scientists are interested in its properties and how they can be harnessed to create new drugs or improve existing ones. (6-chloro-7-methylimidazo[1,2-b]pyridazin-2-yl)acetic acid's potential applications in treating cancer and inflammation are of particular interest, as these are areas with significant unmet medical needs.
Check Digit Verification of cas no
The CAS Registry Mumber 64068-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64068-10:
(7*6)+(6*4)+(5*0)+(4*6)+(3*8)+(2*1)+(1*0)=116
116 % 10 = 6
So 64068-10-6 is a valid CAS Registry Number.
64068-10-6Relevant academic research and scientific papers
Research on heterocyclic compounds. XXXIII-synthesis and analgesic activity of imidazo[1,2-b]pyridazine-2-acetic acid derivatives
Luraschi,Arena,Sacchi,Laneri,Abignente,D'Amico,Berrino,Rossi
, p. 349 - 354 (2007/10/02)
A series of imidazo[1,2-b]pyridazine-2-acetic esters, acids and amides was synthesized and tested for antiinflammatory, analgesic and ulcerogenic activities. The ethyl esters were prepared by cyclocondensation of some 3-aminopyridazines with ethyl 4-chloroacetoacetate, followed by hydrolysis or amminolysis in order to obtain the corresponding acids and amides. The capacity of inhibiting the sarrageenan-induced edema in the rat paw and the writhes induced by acetic acid in mice were evaluated, as well as the ulcerogenic action in rats. The acid is derivatives showed significant analgesic activity which is comparable to that found in other series of imidazo[1,2-b]pyridazine analogs previously examined.
