548769-96-6 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(N-Benzylsulphonamido)benzeneboronic acid is used as a key intermediate in the synthesis of various pharmaceuticals and chemicals. Its unique chemical properties and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Chemical Reactions:
In the field of organic synthesis, 4-(N-Benzylsulphonamido)benzeneboronic acid serves as a reagent in various chemical reactions. Its ability to form stable covalent bonds with other molecules allows for the creation of new compounds with diverse applications.
Used in Enzyme Inhibition:
4-(N-Benzylsulphonamido)benzeneboronic acid has the potential to inhibit the activity of certain enzymes, making it a promising candidate for the development of enzyme-targeting drugs. By modulating enzyme activity, 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID may contribute to the treatment of various diseases and conditions.
Used in Cancer Treatment Research:
4-(N-Benzylsulphonamido)benzeneboronic acid has been studied for its potential therapeutic effects in cancer treatment. Its ability to target and inhibit specific enzymes involved in cancer cell growth and proliferation suggests its potential as a novel anticancer agent. Further research is needed to fully understand its mechanism of action and optimize its use in cancer therapy.
Check Digit Verification of cas no
The CAS Registry Mumber 548769-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,7,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 548769-96:
(8*5)+(7*4)+(6*8)+(5*7)+(4*6)+(3*9)+(2*9)+(1*6)=226
226 % 10 = 6
So 548769-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H14BNO4S/c16-14(17)12-6-8-13(9-7-12)20(18,19)15-10-11-4-2-1-3-5-11/h1-9,15-17H,10H2
548769-96-6Relevant academic research and scientific papers
HALO SULFONYL ARYL BORONATES
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Page 9-10, (2010/02/07)
The present invention relates to halo sulfonyl aryl boronates of the general formula (I): wherein Arylene designates a carbocyclic or heterocyclic, aromatic ring system comprising 1-3 rings; R1, R2 and R3 are, independently, hydrogen, C1-6alkyl, C1-6alkoxy, halogen, nitro, cyano or phenyl;X is fluoro, chloro or bromo; and Y is a boroxine moiety attached via a bond from Arylene to one of the boron atoms of a boroxine ring which ring has a group of the formula -Arylene(R1)(R2)(R3)SO2X, wherein Arylene, R1, R2, R3 and X are as defined above, at each of the other two boron atoms of the boroxine ring, or Y is a boronic acid group or a boronic ester group.The invention also relates to the preparation of the compounds of formula (I) and to their use in organic synthesis.
Halo sulfonyl aryl boronates
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Page 5, (2010/02/07)
The present invention relates to halo sulfonyl aryl boronates of the general formula (I): wherein Arylene designates a carbocyclic or heterocyclic, aromatic ring system comprising 1-3 rings; R1, R2 and R3 are, independentl
