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(3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid is a chemical compound utilized in organic synthesis and medicinal chemistry, characterized by a boronic acid functional group that plays a pivotal role in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds. The presence of fluoro and sulfamoyl groups endows (3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid with distinctive reactivity and selectivity in a range of chemical reactions. It has garnered attention for its potential in drug discovery and development, particularly in the design of innovative pharmaceuticals and agrochemicals. (3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid's diverse chemical properties and potential therapeutic benefits render it an invaluable asset in the realm of organic and medicinal chemistry.

1704095-91-9

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1704095-91-9 Usage

Uses

Used in Organic Synthesis:
(3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid serves as a key intermediate in organic synthesis, particularly for the creation of complex organic molecules through its involvement in Suzuki-Miyaura cross-coupling reactions. Its unique reactivity and selectivity facilitate the formation of carbon-carbon bonds, which are crucial for constructing a variety of organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid is used as a building block for the design and synthesis of novel pharmaceuticals. Its chemical properties allow for the development of new drug candidates with potential therapeutic benefits, contributing to the advancement of treatments for various diseases and conditions.
Used in Drug Discovery and Development:
(3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid is employed in drug discovery and development processes, where its unique structural features and reactivity can lead to the creation of new and effective drug molecules. Its potential applications in this area highlight its importance in the ongoing search for innovative treatments and therapies.
Used in Agrochemicals:
(3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid also finds use in the development of agrochemicals, where its chemical properties can be harnessed to create new pesticides, herbicides, or other agricultural chemicals. This application underscores the versatility of (3-fluoro-4-(N-methylsulfamoyl)phenyl)boronic acid and its broad impact on various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1704095-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1704095-91:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*9)+(3*5)+(2*9)+(1*1)=159
159 % 10 = 9
So 1704095-91-9 is a valid CAS Registry Number.

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