1313040-65-1 Usage
Description
6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester is a chemical compound characterized by the molecular formula C14H21BNO3. It is a derivative of boronic acid pinacol ester, featuring a pyridine ring fused with a hydroxypiperidine group. 6-(4-HYDROXYPIPERIDIN-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER is recognized for its versatile chemical properties and applications across various scientific and industrial fields.
Uses
Used in Organic Synthesis:
6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester serves as a reagent and catalyst in a range of organic reactions. Its ability to facilitate bond formation and transformation makes it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, 6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester is utilized for the development of pharmaceutical compounds. Its unique structure and reactivity contribute to the design and synthesis of potential drug candidates, targeting various therapeutic areas.
Used in Materials Science:
6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester also finds potential applications in materials science. It is employed in the construction of functional materials and polymers, where its chemical properties can be harnessed to create materials with specific characteristics and performance profiles.
Used in Suzuki-Miyaura Coupling:
6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester is used as a catalyst in Suzuki-Miyaura coupling reactions, a widely employed method for the formation of carbon-carbon bonds, particularly in the synthesis of biaryl compounds.
Used in Sonogashira Coupling:
6-(4-HYDROXYPIPERIDIN-1-YL)PYRIDINE-2-BORONIC ACID PINACOL ESTER also acts as a catalyst in Sonogashira coupling, a cross-coupling reaction used to form carbon-carbon bonds, especially in the synthesis of conjugated molecules and polymers.
Used in Stille Coupling:
6-(4-Hydroxypiperidin-1-yl)pyridine-2-boronic acid pinacol ester is utilized in Stille coupling reactions, which are crucial for the formation of carbon-carbon bonds through the reaction of organotin compounds with organic halides or triflates.
Check Digit Verification of cas no
The CAS Registry Mumber 1313040-65-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,0,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1313040-65:
(9*1)+(8*3)+(7*1)+(6*3)+(5*0)+(4*4)+(3*0)+(2*6)+(1*5)=91
91 % 10 = 1
So 1313040-65-1 is a valid CAS Registry Number.
