Product Name:3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isonicotinamide

IUPAC Name:3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-4-carboxamide

CAS:1310384-92-9
Molecular Formula:C12H17BN2O3
Purity:95%
Catalog Number:CM207299
Molecular Weight:248.09

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Product Details

CAS NO:1310384-92-9
Molecular Formula:C12H17BN2O3
Melting Point:-
Smiles Code:O=C(N)C1=CC=NC=C1B2OC(C)(C)C(C)(C)O2
Density:
Catalog Number:CM207299
Molecular Weight:248.09
Boiling Point:
MDL No:
Storage:

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Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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Product Overview 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)isonicotinamide, commonly known as TMI, is a boronic acid derivative that has gained significant attention in the scientific community due to its potential applications in various fields. 
Synthesis Method The synthesis of TMI involves the reaction of 3-aminopyridine with 2-bromo-4,4,5,5-tetramethyl-1,3,2-dioxaborolane in the presence of a palladium catalyst. The resulting compound is then treated with an acid to yield TMI. This synthesis method is relatively simple and efficient, making TMI a readily available compound for research purposes.
Chemical Properties It is relative ease of synthesis, making it readily available for research purposes.
Synthesis and Application It has been shown to exhibit potent inhibitory activity against various enzymes, including proteasomes and kinases, which are involved in the regulation of cellular processes. TMI has also been studied for its potential use as a fluorescent probe for the detection of metal ions.
Future Directions One potential direction is the further exploration of its potential applications in medicinal chemistry, particularly in the development of novel anticancer agents. Additionally, the use of TMI as a fluorescent probe for the detection of metal ions could be further explored. Finally, the development of more efficient synthesis methods for TMI could lead to its wider use in various fields of research.