943153-22-8 Usage
Description
(5-CHLORO-2-METHOXYPYRIDIN-3-YL)BORONIC ACID is a white solid chemical compound that serves as a valuable research chemical. It is primarily utilized in the synthesis of triazine derivatives, which are known to act as phosphodiesterase inhibitors. These derivatives have potential applications in the treatment of various central nervous system (CNS) disorders, metabolic disorders, and other diseases.
Uses
Used in Pharmaceutical Industry:
(5-CHLORO-2-METHOXYPYRIDIN-3-YL)BORONIC ACID is used as a key intermediate in the synthesis of triazine derivatives for the development of phosphodiesterase inhibitors. These inhibitors are crucial for treating CNS disorders, metabolic disorders, and other diseases, as they help regulate the levels of cyclic nucleotides, which play a significant role in various physiological processes.
Used in Research and Development:
In the field of research and development, (5-CHLORO-2-METHOXYPYRIDIN-3-YL)BORONIC ACID is employed as a versatile building block for the creation of novel compounds with potential therapeutic applications. Its unique structure allows for the exploration of new chemical pathways and the discovery of innovative treatments for a wide range of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 943153-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,1,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 943153-22:
(8*9)+(7*4)+(6*3)+(5*1)+(4*5)+(3*3)+(2*2)+(1*2)=158
158 % 10 = 8
So 943153-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7BClNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3,10-11H,1H3
943153-22-8Relevant articles and documents
IMIDAZO [1,2-B] PYRIDAZINE AND IMIDAZO [4,5-B] PYRIDINE DERIVATIVES AS JAK INHIBITORS
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Page/Page column 54, (2012/06/15)
New imidazo[1,2-b]pyridazine and imidazo[4,5-b]pyridine derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Janus Kinases (JAK).