(R)-5-Bromo-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-2-amine

98%

Reagent Code: #71634
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CAS Number 877399-00-3

science Other reagents with same CAS 877399-00-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.04 g/mol
Formula C₁₃H₁₀BrCl₂FN₂O
badge Registry Numbers
MDL Number MFCD18207061
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in pharmaceutical research, particularly in the development of targeted therapies. Its structure suggests potential applications in the inhibition of specific enzymes or receptors, making it a candidate for drug discovery programs. Researchers explore its efficacy in modulating biological pathways associated with diseases such as cancer or inflammatory disorders. Additionally, it may serve as a key intermediate in the synthesis of more complex molecules designed for therapeutic use. Its unique halogenated aromatic components contribute to its ability to interact with biological targets, enhancing its potential as a lead compound in medicinal chemistry.

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Test Parameter Specification
Appearance Almost white to yellow crystal powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿770.00
inventory 1g
10-20 days ฿1,820.00
inventory 5g
10-20 days ฿8,240.00
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(R)-5-Bromo-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-2-amine
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This compound is primarily utilized in pharmaceutical research, particularly in the development of targeted therapies. Its structure suggests potential applications in the inhibition of specific enzymes or receptors, making it a candidate for drug discovery programs. Researchers explore its efficacy in modulating biological pathways associated with diseases such as cancer or inflammatory disorders. Additionally, it may serve as a key intermediate in the synthesis of more complex molecules designed for therapeutic use. Its unique halogenated aromatic components contribute to its ability to interact with biological targets, enhancing its potential as a lead compound in medicinal chemistry.
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