950662-22-3 Usage
Description
(2-chloro-4,5-dimethoxyphenyl)boronic acid is a boronic acid derivative characterized by a chloro-substituted phenyl ring and two methoxy groups. It is a chemical compound that belongs to the class of boronic acids and is known for its unique chemical structure and properties.
Uses
Used in Organic Synthesis:
(2-chloro-4,5-dimethoxyphenyl)boronic acid is used as a reagent in organic synthesis, particularly in the field of medicinal chemistry and drug development. Its unique chemical structure allows it to be a valuable building block for the synthesis of biologically active molecules.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of medicinal chemistry, (2-chloro-4,5-dimethoxyphenyl)boronic acid is used as a reactant in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. This reaction is crucial for the synthesis of complex organic molecules, including pharmaceutical compounds.
Used in Materials Science:
(2-chloro-4,5-dimethoxyphenyl)boronic acid has been researched for its potential applications in materials science. Its unique properties make it a promising candidate for the development of new materials with specific characteristics.
Used in Catalysis:
Additionally, (2-chloro-4,5-dimethoxyphenyl)boronic acid has been explored for its potential use in catalysis. Its unique chemical structure allows it to act as a catalyst in various chemical reactions, contributing to the efficiency and selectivity of these processes.
Check Digit Verification of cas no
The CAS Registry Mumber 950662-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,6,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 950662-22:
(8*9)+(7*5)+(6*0)+(5*6)+(4*6)+(3*2)+(2*2)+(1*2)=173
173 % 10 = 3
So 950662-22-3 is a valid CAS Registry Number.
950662-22-3Relevant articles and documents
Syntheses of the fungal metabolites Boletopsins 7, 11, and 12 from the Papua New Guinea medicinal mushroom Boletopsis sp.
Beekman, Andrew M.,Barrow, Russell A.
, p. 1017 - 1024 (2014/03/21)
Boletopsins 7 (1), 11 (2), and 12 (3) are p-terphenyl dibenzofuran compounds, isolated from the Papua New Guinean medicinal mushroom Boletopsis sp. The first syntheses of these fungal metabolites are reported, allowing for an investigation of their antibiotic activity. The key steps include sequential Suzuki-Miyaura couplings to rapidly form the p-terphenyl backbone and an Ullmann ether synthesis on a formate ester to create the dibenzofuran moiety. Biological evaluation of the synthetic compounds and intermediates against a panel of bacterial nosocomial pathogens was performed.
