176976-42-4 Usage
Description
4-Chloro-3-(trifluoromethyl)phenylboronic acid is an organic compound that features a boron atom bonded to a phenyl ring with a chlorine atom at the 4th position and a trifluoromethyl group at the 3rd position. 4-Chloro-3-(trifluoromethyl)phenylboronic acid is known for its reactivity and stability, making it a valuable building block in the synthesis of various organic molecules, particularly those with biological and pharmacological significance.
Uses
Used in Suzuki Reaction:
4-Chloro-3-(trifluoromethyl)phenylboronic acid is used as a key reagent in the Suzuki reaction, a widely employed method for the formation of carbon-carbon bonds, specifically in the synthesis of biaryl compounds. The reaction involves the cross-coupling of an aryl or vinyl halide with an organoboron compound, such as 4-Chloro-3-(trifluoromethyl)phenylboronic acid, in the presence of a palladium catalyst and a base. This process is highly valuable in the fields of organic chemistry and medicinal chemistry, as it allows for the creation of complex molecular structures with potential applications in various industries.
Used in Pharmaceutical Industry:
4-Chloro-3-(trifluoromethyl)phenylboronic acid is used as an intermediate in the synthesis of biologically and pharmacologically active molecules. Its unique structure and reactivity make it a versatile building block for the development of new drugs and therapeutic agents. The compound can be employed in the design and synthesis of novel compounds with potential applications in the treatment of various diseases and medical conditions.
Used in Chemical Research:
4-Chloro-3-(trifluoromethyl)phenylboronic acid is also used as a research reagent in the field of chemical research. Its unique properties and reactivity make it an attractive candidate for the exploration of new reaction pathways, the development of innovative synthetic methods, and the investigation of novel chemical transformations. 4-Chloro-3-(trifluoromethyl)phenylboronic acid can contribute to the advancement of knowledge in organic chemistry and the discovery of new chemical processes with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 176976-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,7 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176976-42:
(8*1)+(7*7)+(6*6)+(5*9)+(4*7)+(3*6)+(2*4)+(1*2)=194
194 % 10 = 4
So 176976-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H6F3N.ClH/c1-2(7)3(4,5)6;/h2H,7H2,1H3;1H
