488133-21-7 Usage
Uses
Used in Organic Synthesis:
2-(4-(Bromomethyl)phenyl)-1,3,2-dioxaborolane is used as a reagent in Suzuki-Miyaura cross-coupling reactions for the formation of carbon-carbon bonds in organic molecules. Its reactivity, due to the bromomethyl group, facilitates the creation of new molecular structures that are essential in various chemical processes.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2-(4-(Bromomethyl)phenyl)-1,3,2-dioxaborolane is used as a key building block for the synthesis of various drugs. Its ability to form carbon-carbon bonds makes it instrumental in constructing complex molecular structures required for the development of new medications.
Used in Agrochemical Synthesis:
Similarly, in agrochemical synthesis, 2-(4-(Bromomethyl)phenyl)-1,3,2-dioxaborolane is utilized as a building block for creating molecules with pesticidal, herbicidal, or other agricultural applications. Its role in forming carbon-carbon bonds is crucial for the development of effective and targeted agrochemicals.
Used in Fine Chemicals Synthesis:
2-(4-(Bromomethyl)phenyl)-1,3,2-dioxaborolane is also employed in the synthesis of fine chemicals, which are high-purity chemicals used in various industries such as fragrances, dyes, and specialty chemicals. Its reactivity and ability to form carbon-carbon bonds contribute to the creation of complex and high-quality fine chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 488133-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,1,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 488133-21:
(8*4)+(7*8)+(6*8)+(5*1)+(4*3)+(3*3)+(2*2)+(1*1)=167
167 % 10 = 7
So 488133-21-7 is a valid CAS Registry Number.
488133-21-7Relevant academic research and scientific papers
D’Silva, Claudius
, p. 655 - 659 (2021)
The synthesis of 1-(4-boronobenzyl)-1H-pyrrole was investigated using three different routes. Two key routes that involved the introduction of the boronate group protected as the pinacol ester, failed, due to deprotection problems. The route involving the
