N-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-2-phenylacetamide
95%
Reagent
Code: #83839
CAS Number
2103386-32-7
science Other reagents with same CAS 2103386-32-7
blur_circular Chemical Specifications
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Molecular Information
Weight
355.2109232 g/mol
Formula
C₂₀H₂₃BFNO₃
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Registry Numbers
MDL Number
MFCD32206506
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Storage & Handling
Storage
2-8°C
description Product Description
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. These structures are essential in pharmaceutical research for developing new drugs. The compound serves as a key intermediate in producing active pharmaceutical ingredients (APIs) with potential therapeutic applications. Additionally, it is utilized in material science for designing advanced organic materials with specific electronic or optical properties. Its boronate ester group enables precise modifications in molecular frameworks, making it valuable in both medicinal chemistry and material innovation.
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