397843-69-5 Usage
General Description
[3-(N-Isopropylaminocarbonyl)phenyl]boronic acid is a boronic acid derivative with the chemical formula C12H16BNO3. It is a white to off-white solid that is insoluble in water but soluble in organic solvents. [3-(N-Isopropylaminocarbonyl)phenyl]boronic acid is commonly used in organic synthesis as a building block for the production of various pharmaceuticals and agrochemicals. It is also used as a reactant in the Suzuki-Miyaura coupling reaction, a widely utilized method for carbon-carbon bond formation in organic chemistry. Additionally, [3-(N-Isopropylaminocarbonyl)phenyl]boronic acid is being investigated for its potential use in the development of novel treatments for certain diseases, including cancer. Due to its boronic acid functional group, it has the ability to form reversible covalent bonds with certain biological targets, making it an interesting compound for medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 397843-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,7,8,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 397843-69:
(8*3)+(7*9)+(6*7)+(5*8)+(4*4)+(3*3)+(2*6)+(1*9)=215
215 % 10 = 5
So 397843-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BNO3/c1-7(2)12-10(13)8-4-3-5-9(6-8)11(14)15/h3-7,14-15H,1-2H3,(H,12,13)
397843-69-5Relevant articles and documents
Preparation and uses of conjugated solid supports for boronic acids
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, (2008/06/13)
The invention provides novel solid supports comprising dihydroxyalkyl aminoalkyl and dihydroxyalkylaminobenzyl groups, and methods for making and using them. The supports are particularly useful for immobilizing and derivatizing functionalized boronic acids for use in solid phase synthesis, such as those used in combinatorial chemistries. The compositions and methods of the invention are also useful as scavenger solid supports, e.g., in solution-phase parallel synthesis of small molecule libraries, and for use in resin-to-resin transfer reactions via phase transfer of solid supported boronic acids under both aqueous and anhydrous conditions. The methods of the invention provide convergent solid-phase synthesis of symmetrically or unsymmetrically functionalized compounds, such as biphenyl compounds. Also provided are synthesizer devices, e.g., semiautomated parallel synthesizers.
