CAS 2121511-83-7: 2-Bromo-5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description: 2-Bromo-5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a complex organic compound characterized by its heterocyclic structure, which includes a pyridine ring substituted with both bromine and chlorine atoms, as well as a boron-containing moiety. The presence of the bromine and chlorine substituents indicates potential reactivity, making it useful in various synthetic applications, particularly in cross-coupling reactions. The tetramethyl-1,3,2-dioxaborolane group enhances its utility in organoboron chemistry, facilitating the formation of carbon-boron bonds. This compound is likely to exhibit moderate to high stability under standard conditions, but its reactivity can be influenced by the electronic effects of the halogen substituents. Additionally, the presence of the dioxaborolane group suggests potential applications in medicinal chemistry and material science, particularly in the development of new pharmaceuticals or functional materials. As with many organoboron compounds, it may also play a role in catalysis and organic synthesis, contributing to the advancement of green chemistry methodologies.

Formula: C₁₁H₁₄BBrClNO₂

InChI: InChI=1S/C11H14BBrClNO2/c1-10(2)11(3,4)17-12(16-10)8-5-7(14)6-15-9(8)13/h5-6H,1-4H3

InChI key: InChIKey=VCCXYDOXOQYYKI-UHFFFAOYSA-N

SMILES: ClC1=CN=C(Br)C(=C1)B2OC(C)(C)C(O2)(C)C

Synonyms:

• 2-Bromo-5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
• Pyridine, 2-bromo-5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Pyridine, 2-bromo-5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CAS: 2121511-83-7

• Formula: C₁₁H₁₄BBrClNO₂
• Purity: 95%
• Molecular weight: 318.4024

2-Bromo-5-chloropyridine-3-boronic acid pinacol ester

CAS: 2121511-83-7

• Purity: 98%
• Molecular weight: 318.3999938964844