2-(2-Fluoro-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
Reagent
Code: #42439
CAS Number
1073353-89-5
blur_circular Chemical Specifications
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Molecular Information
Weight
267.0600 g/mol
Formula
C₁₂H₁₅BFNO₄
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Registry Numbers
MDL Number
MFCD09264075
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Storage & Handling
Storage
room temperature
description Product Description
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. It is particularly valuable in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it acts as a boron-containing reagent to facilitate the formation of carbon-carbon bonds. This makes it essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its nitro and fluoro substituents make it a versatile building block for designing compounds with specific electronic and steric properties, often used in drug discovery and material science research.
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