2-(2,4-Dinitrophenylthio)benzothiazole

98%

Reagent Code: #174302
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CAS Number 17586-89-9

science Other reagents with same CAS 17586-89-9

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scatter_plot Molecular Information
Weight 333.34 g/mol
Formula C₁₃H₇N₃O₄S₂
badge Registry Numbers
MDL Number MFCD00059704
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a selective colorimetric and fluorogenic chemosensor for detecting thiol-containing compounds, especially cysteine and homocysteine in biological systems. The compound undergoes a nucleophilic aromatic substitution reaction with thiols, resulting in a distinct color change from colorless or pale yellow to deep red or purple, enabling naked-eye detection. This property makes it valuable in biochemical assays and diagnostic tools for monitoring cellular thiol levels. It is also employed in environmental and pharmaceutical analysis due to its high selectivity and sensitivity in aqueous and semi-aqueous media. Additionally, it serves as a building block in the development of smart probes for imaging reactive sulfur species in live cells.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿396.00
inventory 100g
10-20 days ฿2,260.00

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2-(2,4-Dinitrophenylthio)benzothiazole
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Used primarily as a selective colorimetric and fluorogenic chemosensor for detecting thiol-containing compounds, especially cysteine and homocysteine in biological systems. The compound undergoes a nucleophilic aromatic substitution reaction with thiols, resulting in a distinct color change from colorless or pale yellow to deep red or purple, enabling naked-eye detection. This property makes it valuable in biochemical assays and diagnostic tools for monitoring cellular thiol levels. It is also employed i

Used primarily as a selective colorimetric and fluorogenic chemosensor for detecting thiol-containing compounds, especially cysteine and homocysteine in biological systems. The compound undergoes a nucleophilic aromatic substitution reaction with thiols, resulting in a distinct color change from colorless or pale yellow to deep red or purple, enabling naked-eye detection. This property makes it valuable in biochemical assays and diagnostic tools for monitoring cellular thiol levels. It is also employed in environmental and pharmaceutical analysis due to its high selectivity and sensitivity in aqueous and semi-aqueous media. Additionally, it serves as a building block in the development of smart probes for imaging reactive sulfur species in live cells.

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