1048990-22-2 Usage
Uses
Used in Organic Synthesis:
4-bromo-2-(trifluoromethoxy)phenylboronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for versatile reactions, facilitating the creation of complex organic molecules.
Used in Medicinal Research:
In the pharmaceutical industry, 4-bromo-2-(trifluoromethoxy)phenylboronic acid is used as a versatile building block for the development of new drugs. Its ability to form stable bonds with other molecules makes it a promising candidate for the synthesis of bioactive compounds.
Used in Agrochemical Research:
Similarly, in agrochemical research, 4-bromo-2-(trifluoromethoxy)phenylboronic acid is utilized as a building block for the development of new agrochemicals, such as pesticides and herbicides, due to its potential to create stable and effective molecules.
Used in Dye and Electronic Material Development:
4-bromo-2-(trifluoromethoxy)phenylboronic acid is also used in the development of dyes and electronic materials, where its unique properties can contribute to the creation of novel materials with improved performance characteristics.
Used as a Catalyst in Reactions:
In the field of catalysis, 4-bromo-2-(trifluoromethoxy)phenylboronic acid is employed as a catalyst in various reactions, including the Suzuki-Miyaura cross-coupling reactions, which are widely used in the synthesis of biologically active compounds and advanced materials.
Used in Industrial and Commercial Material Development:
Lastly, 4-bromo-2-(trifluoromethoxy)phenylboronic acid has potential applications in the development of new materials for industrial and commercial use, where its unique chemical properties can be leveraged to create innovative products with enhanced performance.
Check Digit Verification of cas no
The CAS Registry Mumber 1048990-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,9,9 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1048990-22:
(9*1)+(8*0)+(7*4)+(6*8)+(5*9)+(4*9)+(3*0)+(2*2)+(1*2)=172
172 % 10 = 2
So 1048990-22-2 is a valid CAS Registry Number.
1048990-22-2Relevant academic research and scientific papers
A general and highly selective chelate-controlled intermolecular oxidative heck reaction
Delcamp, Jared H.,Brucks, Alexandria P.,White, M. Christina
supporting information; scheme or table, p. 11270 - 11271 (2009/02/05)
A novel chelate-controlled intermolecular oxidative Heck reaction is reported that proceeds with a wide range of nonresonance stabilized α-olefin substrates and organoboron reagents to afford internal olefin products in good yields and outstanding regio- and E:Z stereoselectivities. Pd-H isomerization, common in many Heck reactions, is not observed under these mild, oxidative conditions. This is evidenced by outstanding E:Z selectivities (>20:1 in all cases examined), no erosion in optical purity for proximal stereogenic centers, and a tolerance for unprotected alcohols. Remarkably, a single metal/ligand combination, Pd/bis-sulfoxide complex 1, catalyzes this reaction over a broad range of coupling partners. Given the high selectivities and broad scope, we anticipate this intermolecular Heck reaction will find heightened use in complex molecule synthesis. Copyright
