methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxylate


Chemical Name: methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxylate
CAS Number: 1246765-27-4
Product Number: AG000MLB(AGN-PC-09TQ26)
Synonyms:
MDL No:
Molecular Formula: C14H20BNO5
Molecular Weight: 293.1233

Identification/Properties


Computed Properties
Molecular Weight:
293.126g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
293.143g/mol
Monoisotopic Mass:
293.143g/mol
Topological Polar Surface Area:
66.9A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
385
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a key building block in the design and creation of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate acts as a valuable intermediate for the synthesis of complex molecules. Its unique structure and functional groups make it a valuable tool for introducing specific functionalities into target molecules during the synthetic process.One of the key applications of Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate is in the construction of heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. By utilizing this compound in synthetic pathways, chemists can efficiently access a diverse array of heterocyclic structures with tailored properties.Furthermore, Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate enables chemists to perform key transformations such as cross-coupling reactions, allowing for the functionalization of specific positions within a molecule with high selectivity. This versatility makes it a valuable asset in the development of new chemical entities with enhanced biological or material properties.Overall, Methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate is a powerful tool in the hands of synthetic chemists, facilitating the efficient and strategic construction of complex molecules for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.