Product Description:
An organic compound used in various chemical synthesis applications, particularly in Suzuki coupling reactions.
Applications & Uses:
CAS#:
176880-37-8
SYNONYM:
4-Formyl-3-nitrophenylboronic acid pinacol ester;2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
FORMULA:
C13H16BNO5
PRODUCT TYPE:
HAZARD:
Warning
CATEGORIES:
Organic Intermediate
,
Intermediates
,
Research and Development
Technical Specifications
Molecular weight, g/mol :
261.08
2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile chemical compound known for its distinctive structural attributes and wide range of applications in organic synthesis. This compound features a benzaldehyde core substituted with a nitro group and a boronic ester moiety, making it a valuable intermediate in the construction of various complex molecular architectures. It is highly sought after in the pharmaceutical industry for its role in the synthesis of bioactive molecules and active pharmaceutical ingredients. Additionally, its boronate functionality allows for cross-coupling reactions, making it an essential building block in Suzuki-Miyaura cross-coupling reactions, thus facilitating the creation of carbon-carbon bonds with precision and efficiency. This compound''s unique combination of functional groups not only enhances reactivity but also provides chemists with the flexibility to explore novel synthetic pathways and develop new materials. Whether for research and development or industrial applications, 2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a crucial component in the toolkit of innovative chemists aiming to push the boundaries of molecular design and functionality.