886593-45-9 Usage
Uses
Used in Pharmaceutical Development:
4-(2-hydroxypropan-2-yl)phenylboronic acid is used as a key intermediate in the synthesis of novel pharmaceuticals for various therapeutic applications. Its unique structure allows for the creation of new drug candidates with specific binding affinities and biological activities.
Used in Catalyst Design:
In the field of catalysis, 4-(2-hydroxypropan-2-yl)phenylboronic acid is used as a ligand for the design of catalysts that facilitate organic transformations. Its ability to form stable complexes with metal centers contributes to the development of efficient and selective catalytic systems.
Used in Organic Synthesis:
4-(2-hydroxypropan-2-yl)phenylboronic acid is utilized as a reagent in Suzuki-Miyaura cross-coupling reactions, a widely employed method for the formation of carbon-carbon bonds. This application is crucial for the synthesis of complex organic molecules, including natural products and pharmaceutical agents.
Used in Biological Studies:
4-(2-hydroxypropan-2-yl)phenylboronic acid is used as a tool in biological research to study the interactions between small molecules and biomolecules. Its capacity to bind and modulate the activity of specific proteins and enzymes makes it a valuable probe for understanding biological processes and identifying potential therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 886593-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 886593-45:
(8*8)+(7*8)+(6*6)+(5*5)+(4*9)+(3*3)+(2*4)+(1*5)=239
239 % 10 = 9
So 886593-45-9 is a valid CAS Registry Number.
InChI:InChI=1S/C9H13BO3/c1-9(2,11)7-3-5-8(6-4-7)10(12)13/h3-6,11-13H,1-2H3
886593-45-9Relevant academic research and scientific papers
SUBSTITUTED 2-NAPHTHOIC ACIDS AS ANTAGONISTS OF GPR105 ACTIVITY
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Page/Page column 70-71, (2009/07/17)
Substituted 2-naphthoic acids of structural formula I are effective as antagonists of the biological activity of GPR105 protein. They are useful for the treatment, control or prevention of disorders responsive to antagonism of this receptor, such as diabe
PIPERAZINYLPHENALKYL LACTAM/AMINE LIGANDS FOR THE 5HT1B RECEPTOR
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Page/Page column 75-76, (2010/11/30)
The present invention relates to novel derivatives, that are compounds of Formula (I), wherein R1, R2, R3, R14, X, Y, n and m are defined herein, their pharmaceutically acceptable salts, pharmaceutical compositions and methods using said compounds in treating or preventing depression, anxiety, obsessive compulsive disorder (OCD) and other disorders for which selective antagonists, inverse agonists and partial agonists of serotonin 1 (5-HT1) receptors, specifically, antagonists of 5-HT1B are useful.
