1415960-56-3 Usage
Uses
Used in Organic Synthesis:
(4-((tert-butoxycarbonyl)amino)-2-fluorophenyl)boronic acid serves as a versatile building block in organic synthesis, enabling the creation of more intricate organic molecules. Its structure allows for the formation of carbon-carbon and carbon-heteroatom bonds, which is crucial for constructing complex chemical architectures.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-((tert-butoxycarbonyl)amino)-2-fluorophenyl)boronic acid is utilized as a reagent for the development of new pharmaceuticals and bioactive compounds. Its ability to modify and fine-tune the reactivity and selectivity of organic reactions makes it a valuable asset in medicinal chemistry, potentially leading to the discovery of novel therapeutic agents.
Used in the Development of Bioactive Compounds:
Due to its unique structure and reactivity, (4-((tert-butoxycarbonyl)amino)-2-fluorophenyl)boronic acid has potential applications in the development of bioactive compounds. Its role in enhancing the properties of organic reactions can contribute to the synthesis of new molecules with specific biological activities, which may have applications in various fields, including medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 1415960-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,9,6 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1415960-56:
(9*1)+(8*4)+(7*1)+(6*5)+(5*9)+(4*6)+(3*0)+(2*5)+(1*6)=163
163 % 10 = 3
So 1415960-56-3 is a valid CAS Registry Number.
1415960-56-3Relevant academic research and scientific papers
CERTAIN CHEMICAL ENTITIES, COMPOSITIONS, AND METHODS
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Paragraph 0229, (2014/05/24)
Chemical entities that are kinase inhibitors, pharmaceutical compositions and methods of treatment of cancer are described.
