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4-Aminophenylboronic acid pinacol ester

Catalog No.
C6222
A biochemical reagent used to study protein interactions and regulate metabolism.
Grouped product items
SizePriceStock Qty
5g
$50.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

4-Aminophenylboronic acid pinacol ester (CAS No.: 214360-73-3) is a small-molecule boronic ester widely utilized as a versatile biochemical reagent and synthetic intermediate in life science and medicinal chemistry research. Functionally, it serves as a reactive building block for the generation of bioactive compounds, including kinase-targeting scaffolds such as receptor tyrosine kinase inhibitors and derivatives that modulate cyclin-dependent kinases and casein kinase pathways, thereby contributing to studies of cell cycle regulation, proliferation, and oncogenic signaling. Through its ability to participate in target-oriented synthesis and molecular modification, it supports the exploration of protein–ligand interactions and the development of compounds capable of modulating enzymatic activity and intracellular signaling cascades. Although direct biological activity data for this compound are limited, related boronic ester derivatives are commonly associated with enzyme interaction profiles and screening activities in the nanomolar to micromolar range. In experimental settings, it is frequently applied in in vitro biochemical assays, cell-based mechanistic studies, and early-stage drug discovery workflows, where dosing and concentration parameters are adjusted according to specific assay conditions and research objectives. Its utility is particularly relevant in studies of kinase signaling, metabolic regulation, and anticancer drug development.

Chemical Properties

Physical AppearanceA solid
Storage-20°C
M.Wt219.09
Cas No.214360-73-3
FormulaC12H18BNO2
Synonyms4-Aminophenylboronic Acid pinacol ester
Solubilityinsoluble in H2O; ≥11.8 mg/mL in EtOH; ≥19.5 mg/mL in DMSO
Chemical Name4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Canonical SMILESNC1=CC=C(B2OC(C)(C)C(C)(C)O2)C=C1
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

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