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(3-(dibenzylamino)-4-fluorophenyl)boronic acid is a chemical compound with the molecular formula C20H19BFNO2. It belongs to the class of boronic acids and contains a boron atom bonded to a phenyl ring with a fluorine substituent and an amino group. (3-(dibenzylaMino)-4-fluorophenyl)boronic acid is characterized by its ability to form stable complexes with biological molecules, making it a versatile building block in various fields.

1704069-71-5

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1704069-71-5 Usage

Uses

Used in Organic Synthesis:
(3-(dibenzylamino)-4-fluorophenyl)boronic acid is used as a reagent in the field of organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions. These reactions are a powerful method for creating carbon-carbon bonds, which are essential in the construction of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (3-(dibenzylamino)-4-fluorophenyl)boronic acid is used as a key intermediate in the synthesis of various drugs. Its ability to form stable complexes with biological molecules makes it a valuable component in the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, (3-(dibenzylamino)-4-fluorophenyl)boronic acid is utilized as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its interaction with biological molecules can lead to the development of more effective and targeted agrochemicals.
Used in Materials Science:
(3-(dibenzylamino)-4-fluorophenyl)boronic acid also has potential applications in materials science. Its unique chemical properties and ability to form stable complexes can be exploited to create new materials with specific properties, such as improved conductivity or enhanced mechanical strength.
Used in Catalysis:
In the field of catalysis, (3-(dibenzylamino)-4-fluorophenyl)boronic acid can be used as a catalyst or a catalyst precursor. Its ability to form stable complexes with other molecules can facilitate various chemical reactions, making it a valuable tool in the development of new catalytic processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1704069-71-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1704069-71:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*9)+(2*7)+(1*1)=155
155 % 10 = 5
So 1704069-71-5 is a valid CAS Registry Number.

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1704069-71-5Downstream Products

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