2087452-50-2 Usage
Uses
Used in Organic Synthesis:
(5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid is utilized as a building block in organic synthesis for constructing more complex molecules. Its unique structure and functional groups make it a valuable component in the creation of various organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid serves as a precursor for the development of pharmaceuticals and agrochemicals. Its structural properties and reactivity contribute to the design and synthesis of novel therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
(5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid is employed as a valuable reagent in Suzuki-Miyaura cross-coupling reactions. The boronic acid group in (5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid enables the formation of carbon-carbon bonds, which are crucial for the synthesis of various organic molecules and pharmaceuticals.
Used in Drug Discovery:
(5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid's versatility and reactivity make it an essential tool in drug discovery, where it can be used to create new molecules with potential therapeutic properties. Its applications in this field are diverse, ranging from the development of new drugs to the improvement of existing ones.
Used in Chemical Research:
(5-chlorobenzo[d][1,3]dioxol-4-yl)boronic acid is also used in chemical research to study the properties and reactions of boronic acid derivatives. This helps researchers gain a deeper understanding of the compound's potential applications and limitations in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 2087452-50-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,8,7,4,5 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2087452-50:
(9*2)+(8*0)+(7*8)+(6*7)+(5*4)+(4*5)+(3*2)+(2*5)+(1*0)=172
172 % 10 = 2
So 2087452-50-2 is a valid CAS Registry Number.
2087452-50-2Relevant academic research and scientific papers
Takahashi, Shunya,Suda, Yasuaki,Nakamura, Takemichi,Matsuoka, Koji,Koshino, Hiroyuki
, p. 3159 - 3166 (2017)
This paper describes a general method for the synthesis of kehokorins A-E, novel cytotoxic p-terphenyls. 2,4,6-Trihydroxybenzaldehyde served as a common building block for preparation of the central aromatic ring. Construction of their p-terphenyl skeletons was achieved by a stepwise Suzuki-Miyaura coupling, whereas the phenyldibenzofuran moiety was built up by an intramolecular Ullmann reaction. Introduction of an l-rhamnose residue into partly protected kehokorin B was performed by the trichloroacetimidate method.
