4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
≥95%
Reagent
Code: #119422
CAS Number
882670-69-1
science Other reagents with same CAS 882670-69-1
blur_circular Chemical Specifications
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Molecular Information
Weight
233.11 g/mol
Formula
C₁₃H₂₀BNO₂
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Registry Numbers
MDL Number
MFCD05663859
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Physical Properties
Boiling Point
366.2°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
Used in organic synthesis as a key intermediate for the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules. The compound’s boronate ester group enhances its reactivity and selectivity in these reactions. Additionally, it serves as a building block in the development of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce functional groups into aromatic systems. Its applications also extend to the field of medicinal chemistry, where it is utilized in the synthesis of drug candidates targeting various diseases.
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