1257793-03-5 Usage
Description
(3,5-Difluoro-4-iodophenyl)boronic acid is a boronic acid derivative with the molecular formula C6H4BFINF2O2. It features a boron atom bonded to a phenyl ring, which is substituted with fluorine and iodine atoms. (3,5-Difluoro-4-iodophenyl)boronic acid is known for its utility in various chemical reactions and its potential applications in different fields.
Used in Pharmaceutical Industry:
(3,5-Difluoro-4-iodophenyl)boronic acid is used as a synthetic intermediate for the development of pharmaceuticals. Its unique structure allows it to bind to biological targets, facilitating the creation of new chemical entities with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical field, (3,5-Difluoro-4-iodophenyl)boronic acid is used as a building block in the synthesis of agrochemicals. Its ability to form stable bonds with other molecules makes it a valuable component in the development of effective crop protection agents.
Used in Organic Synthesis:
(3,5-Difluoro-4-iodophenyl)boronic acid is used as a reagent in organic synthesis, particularly in the Suzuki-Miyaura coupling reaction. This reaction is crucial for the formation of carbon-carbon bonds, which are essential in constructing complex organic molecules.
Used in Materials Science:
This boronic acid derivative has potential applications in materials science. Its unique properties may contribute to the development of new materials with specific characteristics, such as improved conductivity or stability.
Used as a Building Block in Organic Compounds Synthesis:
(3,5-Difluoro-4-iodophenyl)boronic acid serves as a versatile building block in the synthesis of various organic compounds. Its presence in a molecule can influence the reactivity and properties of the final product, making it a valuable component in the creation of diverse chemical structures.
Check Digit Verification of cas no
The CAS Registry Mumber 1257793-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,7,9 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1257793-03:
(9*1)+(8*2)+(7*5)+(6*7)+(5*7)+(4*9)+(3*3)+(2*0)+(1*3)=185
185 % 10 = 5
So 1257793-03-5 is a valid CAS Registry Number.
1257793-03-5Relevant articles and documents
Electrophilic ipso-iodination of silylated arylboronic acids
Durka,Górka,Kurach,Luliński,Serwatowski
experimental part, p. 2635 - 2643 (2010/11/21)
Silylated functionalized arylboronic acids were converted into corresponding iodinated arylboronic acids in good yields via the electrophilic ipso-desilylation effected with iodine chloride in refluxing CHCl3. Disilylated arylboronic acids were susceptible to diiodination. In addition, the structural characterization and reactivity of a novel sterically hindered ortho-silylated diarylborinic ester were reported. The potential of selected iodinated phenylboronic acids as monomers for the Suzuki-Miyaura cross-coupling polymerization was demonstrated.
