2-((2-Hydroxyethyl)thio)-3-methylnaphthalene-1,4-dione

95%

Reagent Code: #196433
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CAS Number 59147-84-1

science Other reagents with same CAS 59147-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.30 g/mol
Formula C₁₃H₁₂O₃S
badge Registry Numbers
MDL Number MFCD11100314
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of anticoagulant compounds and biologically active naphthoquinone derivatives. It plays a role in the development of pharmaceuticals targeting blood clotting disorders due to its structural similarity to vitamin K antagonists. Also investigated for its potential in electrochemical applications, such as redox mediators in biosensors, owing to the quinone moiety’s reversible electron transfer properties. Additionally, it serves as a building block in the preparation of dyes and fluorescent probes for biochemical labeling.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,700.00
inventory 250mg
10-20 days ฿10,930.00
inventory 1g
10-20 days ฿34,680.00

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2-((2-Hydroxyethyl)thio)-3-methylnaphthalene-1,4-dione
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Used primarily as an intermediate in the synthesis of anticoagulant compounds and biologically active naphthoquinone derivatives. It plays a role in the development of pharmaceuticals targeting blood clotting disorders due to its structural similarity to vitamin K antagonists. Also investigated for its potential in electrochemical applications, such as redox mediators in biosensors, owing to the quinone moiety’s reversible electron transfer properties. Additionally, it serves as a building block in the prep
Used primarily as an intermediate in the synthesis of anticoagulant compounds and biologically active naphthoquinone derivatives. It plays a role in the development of pharmaceuticals targeting blood clotting disorders due to its structural similarity to vitamin K antagonists. Also investigated for its potential in electrochemical applications, such as redox mediators in biosensors, owing to the quinone moiety’s reversible electron transfer properties. Additionally, it serves as a building block in the preparation of dyes and fluorescent probes for biochemical labeling.
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