957060-94-5 Usage
Uses
Used in Organic Synthesis:
5-Bromo-2-methoxypyridin-4-ylboronic acid is used as a reagent in the Suzuki-Miyaura cross-coupling reaction, a widely employed method for forming carbon-carbon bonds. This reaction is crucial for the synthesis of complex organic molecules, including those with potential pharmaceutical or industrial applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Bromo-2-methoxypyridin-4-ylboronic acid serves as a key intermediate for the synthesis of various bioactive compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Drug Development:
5-Bromo-2-methoxypyridin-4-ylboronic acid is utilized as a building block in the preparation of diverse organic molecules, which are essential in the discovery and development of new drugs. Its versatility in chemical reactions facilitates the creation of novel molecular entities with potential therapeutic benefits.
Used in Material Science:
Although not explicitly mentioned in the provided materials, given its structural features and reactivity, 5-Bromo-2-methoxypyridin-4-ylboronic acid may also find applications in material science, particularly in the design of new materials with specific properties, such as conductivity, stability, or catalytic activity.
Check Digit Verification of cas no
The CAS Registry Mumber 957060-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 957060-94:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*0)+(2*9)+(1*4)=195
195 % 10 = 5
So 957060-94-5 is a valid CAS Registry Number.
957060-94-5Relevant academic research and scientific papers
Parry, Paul R.,Bryce, Martin R.,Tarbit, Brian
, p. 1035 - 1038 (2003)
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);
