182344-23-6 Usage
Description
4-Fluoro-3-(trifluoromethyl)phenylboronic acid is an organic compound that serves as a valuable intermediate in the synthesis of various organic molecules. It is characterized by its white solid appearance and is known for its reactivity in chemical reactions, particularly in the Suzuki reaction.
Uses
Used in Organic Chemical Synthesis:
4-Fluoro-3-(trifluoromethyl)phenylboronic acid is used as an organic chemical synthesis intermediate for the production of a wide range of organic compounds. Its unique structure allows it to participate in various chemical reactions, enabling the creation of diverse molecules with potential applications in different industries.
Used in the Suzuki Reaction:
In the field of organic chemistry, 4-Fluoro-3-(trifluoromethyl)phenylboronic acid is utilized as a key component in the Suzuki reaction. This cross-coupling reaction is widely employed for the formation of carbon-carbon bonds, which are essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
4-Fluoro-3-(trifluoromethyl)phenylboronic acid is used as a building block in the development of new pharmaceutical compounds. Its unique structure and reactivity make it a valuable asset in the design and synthesis of novel drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Fluoro-3-(trifluoromethyl)phenylboronic acid is employed in the synthesis of new agrochemical products, such as pesticides and herbicides. Its involvement in the creation of these compounds can lead to the development of more effective and environmentally friendly solutions for agricultural challenges.
Used in Advanced Materials:
4-Fluoro-3-(trifluoromethyl)phenylboronic acid is also used in the development of advanced materials, such as polymers and composites, with unique properties. These materials can find applications in various sectors, including electronics, aerospace, and automotive industries, where high-performance materials are in demand.
Check Digit Verification of cas no
The CAS Registry Mumber 182344-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,4 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182344-23:
(8*1)+(7*8)+(6*2)+(5*3)+(4*4)+(3*4)+(2*2)+(1*3)=126
126 % 10 = 6
So 182344-23-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BF4O2/c9-6-2-1-4(8(13)14)3-5(6)7(10,11)12/h1-3,13-14H
182344-23-6Relevant articles and documents
Sterically encumbered fluorene-based poly(arylene ether)s containing spiro-annulated substituents on the main chain
Huang, Wen Y.,Huang
scheme or table, p. 10355 - 10365 (2011/09/13)
Two novel fluorene-based bisphenol monomers containing spiro-annulated substituents on the middle biphenylene moiety have been synthesized in this study. Through reacting with four 2-trifluoromethyl-activated bisfluoro monomers, two monomers were converted into a series of fluorene-based poly(arylene ether)s by nucleophilic displacement of the fluorine atoms on the terminal benzene ring of bisfluoro monomers. The obtained polymers exhibit weight-average molecular weight up to 2.41 × 105 g/mol in GPC. Thermal analysis studies indicated that these polymers did not show melting endotherms but did show ultrahigh Tg values up to 356 °C in DSC and outstanding thermal stability up to 643 °C for 5% weight loss in TGA under nitrogen atmosphere. The polymers are soluble in a wide range of organic solvents, THF, CHCl3, NMP, DMAc, DMF, toluene, etc., and are insoluble in DMSO and acetone at room temperature. Transparent and flexible films were easily prepared by solution casting from chloroform solution of each of the polymers.
