612845-44-0 Usage
Uses
Used in Organic Synthesis:
(6-Ethoxypyridin-3-yl)boronic acid is used as a building block for the creation of various biologically active molecules and pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-Ethoxypyridin-3-yl)boronic acid is utilized for its potential to form complex molecular structures that can target specific biological pathways, thereby enhancing the discovery of novel pharmaceuticals.
Used in Pharmaceutical Research:
(6-Ethoxypyridin-3-yl)boronic acid is employed as a reagent in Suzuki and Miyaura cross-coupling reactions, which are pivotal transformations in organic synthesis. These reactions facilitate the formation of new carbon-carbon bond connections, essential for the synthesis of complex organic molecules with potential pharmaceutical applications.
Used in Drug Development:
(6-Ethoxypyridin-3-yl)boronic acid is used as a precursor in the development of new drugs, where its unique structural features can be leveraged to design molecules with improved pharmacological properties, such as enhanced potency, selectivity, and bioavailability.
Used in Chemical Research:
In the broader scope of chemical research, (6-Ethoxypyridin-3-yl)boronic acid serves as a model compound for studying the reactivity and selectivity of boronic acids in various chemical reactions, providing insights into the underlying mechanisms and guiding the design of new synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 612845-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,8,4 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 612845-44:
(8*6)+(7*1)+(6*2)+(5*8)+(4*4)+(3*5)+(2*4)+(1*4)=150
150 % 10 = 0
So 612845-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10BNO3/c1-2-12-7-4-3-6(5-9-7)8(10)11/h3-5,10-11H,2H2,1H3
612845-44-0Relevant academic research and scientific papers
New shelf-stable halo- and alkoxy-substituted pyridylboronic acids and their suzuki cross-coupling reactions to yield heteroarylpyridines
Parry, Paul R.,Bryce, Martin R.,Tarbit, Brian
, p. 1035 - 1038 (2007/10/03)
New shelf-stable pyridylboronic acids have been synthesized: bromine-lithium exchange followed by reaction with triisopropylborate (TIPB) yielded 2-fluoro-5-pyridylboronic acid (4), 3-bromo-5-pyridylboronic acid (5) and 2-ethoxy-5-pyridylboronic acid (6);
