2-(dimethylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbonitrile


Chemical Name: 2-(dimethylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbonitrile
CAS Number: 1346809-50-4
Product Number: AG009BS3(AGN-PC-09PZOP)
Synonyms:
MDL No:
Molecular Formula: C14H20BN3O2
Molecular Weight: 273.1385

Identification/Properties


Computed Properties
Molecular Weight:
273.143g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
273.165g/mol
Monoisotopic Mass:
273.165g/mol
Topological Polar Surface Area:
58.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
400
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



2-(Dimethylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile is a specialized compound commonly utilized in chemical synthesis processes. Its unique chemical structure allows for versatile applications in various synthetic pathways, particularly in the field of organic chemistry. This compound serves as a valuable building block in the creation of complex molecules and functional materials due to its reactivity and compatibility with a wide range of chemical reactions. Specifically, its incorporation into organic synthesis enables the generation of novel compounds with enhanced properties and potential applications in pharmaceuticals, agrochemicals, and materials science. By acting as a key intermediate in synthetic routes, 2-(Dimethylamino)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile plays a crucial role in advancing the development of cutting-edge substances and facilitating the exploration of new chemical entities.