918138-36-0 Usage
Description
5-(Pyridin-3-yloxy)pyridine-3-boronic acid is a chemical compound with the formula C11H9BNO3. It is a boronic acid derivative featuring a pyridine core and a pyridin-3-yloxy group attached to it. 5-(Pyridin-3-yloxy)pyridine-3-boronic acid is known for its ability to form stable complexes with diols and other Lewis bases, which makes it a versatile chemical building block with potential applications in various fields.
Uses
Used in Organic Synthesis:
5-(Pyridin-3-yloxy)pyridine-3-boronic acid is used as a reagent for the formation of carbon-carbon and carbon-nitrogen bonds in organic synthesis. Its unique structure allows for additional reactivity and selectivity in certain types of reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Sensor Development:
Due to its ability to form stable complexes with Lewis bases, 5-(Pyridin-3-yloxy)pyridine-3-boronic acid is used as a component in the development of sensors. Its interactions with various compounds can be harnessed to create sensitive and selective detection methods for a range of target molecules.
Used in Catalyst Design:
5-(Pyridin-3-yloxy)pyridine-3-boronic acid's capacity to form stable complexes also makes it useful in the design of catalysts. 5-(Pyridin-3-yloxy)pyridine-3-boronic acid can be incorporated into catalyst structures to enhance their activity and selectivity in various chemical reactions, contributing to more efficient and environmentally friendly processes.
Used in Medicinal Chemistry:
The presence of the pyridin-3-yloxy group in 5-(Pyridin-3-yloxy)pyridine-3-boronic acid may confer specific reactivity and selectivity that can be exploited in the development of new pharmaceutical agents. This makes the compound a promising candidate for use in medicinal chemistry, where it could contribute to the discovery of novel drugs and therapeutic agents.
Used in Materials Science:
5-(Pyridin-3-yloxy)pyridine-3-boronic acid's versatility and reactivity also make it a candidate for use in materials science. It can be used to develop new materials with unique properties, such as improved conductivity, stability, or responsiveness to environmental stimuli, which can be applied in various high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 918138-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,3 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 918138-36:
(8*9)+(7*1)+(6*8)+(5*1)+(4*3)+(3*8)+(2*3)+(1*6)=180
180 % 10 = 0
So 918138-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9BN2O3/c14-11(15)8-4-10(7-13-5-8)16-9-2-1-3-12-6-9/h1-7,14-15H
918138-36-0Relevant articles and documents
Novel oxybispyridylboronic acids: synthesis and study of their reactivity in Suzuki-type cross-coupling reactions
Voisin, Anne Sophie,Bouillon, Alexandre,Berenguer, Inmaculada,Lancelot, Jean-Charles,Lesnard, Aurélien,Rault, Sylvain
, p. 11734 - 11739 (2006)
This paper sets forth the synthesis of novel oxybispyridylboronic acids, which are prepared from the corresponding halo-oxybispyridines via halogen-metal exchange using n-butyllithium and treatment with triisopropylborate. A range of efficient cross-coupl
