2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbaldehyde


Chemical Name: 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbaldehyde
CAS Number: 1310384-06-5
Product Number: AG000VDV(AGN-PC-086F9K)
Synonyms:
MDL No:
Molecular Formula: C12H15BFNO3
Molecular Weight: 251.0618

Identification/Properties


Safety Information


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

NMR Spectrum


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Chemical Structure



2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is frequently used in the preparation of various advanced materials and pharmaceutical intermediates. Its unique structure allows for precise modifications and substitutions, making it a valuable tool in organic synthesis.In chemical reactions, 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde serves as a key starting material for the creation of complex molecules with specific functional groups. Its ability to participate in numerous reactions, such as cross-coupling, nucleophilic addition, and condensation reactions, enables the synthesis of diverse chemical compounds with tailored properties.Furthermore, the presence of the fluoro and dioxaborolane groups in $name$ enhances its reactivity and stability, making it an ideal candidate for challenging transformations. Chemists leverage these characteristics to achieve precise control over the formation of chemical bonds and stereochemistry, leading to efficient and selective syntheses of target molecules.Overall, 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde is a valuable tool in chemical synthesis, facilitating the development of novel materials and pharmaceuticals through its versatile reactivity and structural properties.