281232-88-0 Usage
Uses
Used in Pharmaceutical Industry:
4-(6-Methoxypyridazin-3-yl)benzoic acid is used as a building block for the synthesis of bioactive molecules, leveraging its unique chemical structure to create new pharmaceutical agents. Its potential applications in this industry may include the development of drugs targeting various diseases and conditions, given the compound's ability to interact with biological systems.
Used in Materials Science:
In the field of materials science, 4-(6-Methoxypyridazin-3-yl)benzoic acid is utilized as a component in the development of new materials with specific properties. Its incorporation into material formulations can lead to the creation of advanced materials with tailored characteristics, such as improved stability, reactivity, or selectivity, depending on the desired application.
Further research and testing are necessary to fully understand the potential uses and effects of 4-(6-Methoxypyridazin-3-yl)benzoic acid in these industries, as well as to identify any additional applications where its unique properties can be harnessed for beneficial outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 281232-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,2,3 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 281232-88:
(8*2)+(7*8)+(6*1)+(5*2)+(4*3)+(3*2)+(2*8)+(1*8)=130
130 % 10 = 0
So 281232-88-0 is a valid CAS Registry Number.
281232-88-0Relevant articles and documents
SUBSTITUTED (AMINOIMINOMETHYL OR AMINOMETHYL) BENZOHETEROARYL COMPOUNDS
-
, (2008/06/13)
This invention is directed to an (aminoiminomethyl or aminomethyl) benzoheteroaryl compound of formula I which is useful for inhibiting the activity of Factor Xa by combining said compound with a composition containing Factor Xa. The present invention is also directed to compositions containing compounds of the formula I, methods for their preparation, their use, such as in inhibiting the formation of thrombin or for treating a patient suffering from, or subject to, a disease state associated with a physiologically detrimental excess amount of thrombin.
A convenient synthesis of heteroaryl benzoic acids via Suzuki reaction
Gong, Yong,Pauls, Henry W.
, p. 829 - 831 (2007/10/03)
An one step approach to heteroaryl benzoic acids from readily accessible heteroaryl halides and carboxybenzene boronic acids is described. The Suzuki coupling is carried out in the presence of Pd(PPh3)4 and sodium carbonate in aqueous acetonitrile. The scope and limitations of the reaction are discussed.
