2-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
98%
Reagent
Code: #219627
CAS Number
1268163-62-7
blur_circular Chemical Specifications
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Molecular Information
Weight
277.08 g/mol
Formula
C₁₃H₁₆BNO₅
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Registry Numbers
MDL Number
MFCD22493668
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Storage & Handling
Storage
Room temperature, inert gas
description Product Description
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex aromatic aldehydes, which are valuable in pharmaceutical and agrochemical industries. The boronate ester group facilitates coupling with aryl halides, while the aldehyde group allows further functionalization, such as reduction or imine formation. Its nitro group can be selectively reduced to an amine, enabling access to multifunctional building blocks for drug discovery and materials science. Commonly employed in the development of organic semiconductors and bioactive molecules.
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