850568-34-2 Usage
Uses
Used in Organic Synthesis:
3-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID is used as a reagent for the Suzuki-Miyaura coupling reaction, which is essential for forming carbon-carbon bonds in organic chemistry. This reaction is widely utilized due to its versatility and the stability of the bonds it forms, making it a cornerstone in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the field of medicinal chemistry, 3-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID is used as a component in the development of pharmaceutical agents. Its role is particularly significant in cancer research, where it has demonstrated potential as a therapeutic agent. The piperidine-1-carbonyl group's ability to improve the compound's cellular uptake and distribution makes it a valuable asset in the creation of drugs that can effectively target and treat cancer cells.
Used in Cancer Research:
3-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID is used as a research tool in cancer research for its potential as a therapeutic agent. 3-(PIPERIDINE-1-CARBONYL)PHENYLBORONIC ACID's structural features allow for enhanced interaction with biological targets, which can lead to the development of new drugs that are more effective in combating cancer. Its application in this field is driven by the need for innovative and targeted cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 850568-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 850568-34:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*8)+(2*3)+(1*4)=182
182 % 10 = 2
So 850568-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H16BNO3/c15-12(14-7-2-1-3-8-14)10-5-4-6-11(9-10)13(16)17/h4-6,9,16-17H,1-3,7-8H2
