1-ethyl-4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazine


Chemical Name: 1-ethyl-4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazine
CAS Number: 940285-00-7
Product Number: AG00IHXE(AGN-PC-09SI5M)
Synonyms:
MDL No:
Molecular Formula: C17H28BN3O2
Molecular Weight: 317.2341

Identification/Properties


Computed Properties
Molecular Weight:
317.24g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
317.227g/mol
Monoisotopic Mass:
317.227g/mol
Topological Polar Surface Area:
37.8A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
395
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



1-Ethyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine is a versatile compound widely employed in chemical synthesis, particularly in the field of organic chemistry. With its unique structure and reactivity, this compound serves as a valuable building block for the creation of various complex molecules.One significant application of 1-Ethyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine lies in its utility as a coupling reagent in the synthesis of organic compounds. In this role, it acts as a key component in cross-coupling reactions, facilitating the formation of carbon-carbon or carbon-heteroatom bonds. This enables chemists to construct intricate molecular structures with precision and efficiency.Furthermore, the presence of the dioxaborolane moiety in 1-Ethyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine enhances its functionality as a versatile synthetic intermediate. The boron atom in the dioxaborolane group can participate in various transformations, such as Suzuki-Miyaura coupling reactions, enabling the selective modification of organic molecules in a controlled manner.Overall, the strategic incorporation of 1-Ethyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine in chemical synthesis processes showcases its significance as a valuable tool for the construction of complex and diverse molecular architectures.