N,N-Dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
98%
Reagent
Code: #219653
CAS Number
325142-87-8
blur_circular Chemical Specifications
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Molecular Information
Weight
247.14 g/mol
Formula
C₁₄H₂₂BNO₂
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Registry Numbers
MDL Number
MFCD06795669
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Storage & Handling
Storage
Room temperature, inert gas
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in the preparation of complex aromatic amines found in bioactive molecules. Due to the stability and reactivity of the boronate ester, it is widely employed in medicinal chemistry for late-stage functionalization of aromatic systems. Additionally, it finds use in materials science for constructing conjugated organic frameworks used in optoelectronic devices.
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