2,4-Dibromo-6-[(E)-[[(1R,2R)-2-(isoindolin-2-yl)-1,2-diphenylethyl]imino]methyl]phenol

93%

Reagent Code: #174413
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CAS Number 1420042-07-4

science Other reagents with same CAS 1420042-07-4

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Weight ?576.33 g/mol
Formula C₂₉H₂₄Br₂N₂O
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a specialized fluorescent probe in biochemical research due to its strong emission properties upon binding to specific metal ions. It is particularly effective in detecting zinc and copper in cellular environments, enabling real-time imaging in live cells. Its structure allows for high selectivity and low detection limits, making it valuable in studying metal ion homeostasis. Also employed in the development of chemosensors for environmental monitoring, where it helps identify trace metal contaminants in water samples. The compound’s imine and phenolic groups contribute to its chelating ability, enhancing sensitivity and stability in sensing applications.

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inventory 10mg
10-20 days ฿4,140.00

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2,4-Dibromo-6-[(E)-[[(1R,2R)-2-(isoindolin-2-yl)-1,2-diphenylethyl]imino]methyl]phenol
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Used as a specialized fluorescent probe in biochemical research due to its strong emission properties upon binding to specific metal ions. It is particularly effective in detecting zinc and copper in cellular environments, enabling real-time imaging in live cells. Its structure allows for high selectivity and low detection limits, making it valuable in studying metal ion homeostasis. Also employed in the development of chemosensors for environmental monitoring, where it helps identify trace metal contami

Used as a specialized fluorescent probe in biochemical research due to its strong emission properties upon binding to specific metal ions. It is particularly effective in detecting zinc and copper in cellular environments, enabling real-time imaging in live cells. Its structure allows for high selectivity and low detection limits, making it valuable in studying metal ion homeostasis. Also employed in the development of chemosensors for environmental monitoring, where it helps identify trace metal contaminants in water samples. The compound’s imine and phenolic groups contribute to its chelating ability, enhancing sensitivity and stability in sensing applications.

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