1217501-18-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Research:
2-Bromo-5-chlorophenylboronic acid is used as a building block for the synthesis of biologically active molecules, playing a crucial role in the development of new drugs and agrochemicals. Its unique structure allows for the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction, which is essential for constructing diverse and complex molecular frameworks.
Used in Organic Synthesis:
2-Bromo-5-chlorophenylboronic acid is used as a reagent in organic synthesis, particularly for the Suzuki-Miyaura cross-coupling reaction. This reaction is a powerful tool for forming carbon-carbon bonds, enabling the creation of a wide range of organic compounds with potential applications in various fields.
Used in Materials Science:
2-Bromo-5-chlorophenylboronic acid is used as a precursor in the development of organic electronic devices and advanced polymers. Its ability to form stable and functional molecular structures makes it a valuable component in the design and synthesis of materials with specific electronic, optical, or mechanical properties.
Used in the Production of Complex Chemicals:
2-Bromo-5-chlorophenylboronic acid is considered a valuable intermediate for the production of various complex chemicals with diverse applications. Its unique structure and reactivity make it an essential component in the synthesis of specialty chemicals, fine chemicals, and other advanced chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 1217501-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,5,0 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1217501-18:
(9*1)+(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*1)+(1*8)=112
112 % 10 = 2
So 1217501-18-2 is a valid CAS Registry Number.
1217501-18-2Relevant academic research and scientific papers
Dherbassy, Quentin,Lanzi, Matteo,Wencel-Delord, Joanna
, p. 14852 - 14857 (2021)
Despite the widespread application of hypervalent iodines, the corresponding λ3-bromanes are less explored. Herein we report a general, safe, and high-yielding strategy to access cyclic diaryl λ3-bromanes. These unique compounds feature reactivity that is appealing and complementary to that of λ3-iodanes, generating arynes under mild reaction conditions and in the presence of a weak base. Accordingly, formal meta-selective transition-metal-free C–O and C–N couplings may be achieved. Mechanistic studies unambiguously support the aryne generation mechanism.
