3-Bromo-6-nitroquinoline

95%

Reagent Code: #118063
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CAS Number 7101-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.05 g/mol
Formula C₉H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD12024480
thermostat Physical Properties
Boiling Point 369.7±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of more complex quinoline derivatives. Its bromo and nitro functional groups make it a versatile building block for various chemical reactions, including nucleophilic substitution and reduction processes. It is often employed in the development of pharmaceutical compounds, particularly those targeting infectious diseases, due to the biological activity associated with quinoline structures. Additionally, it finds application in the synthesis of dyes and pigments, where its nitro group contributes to color formation. Researchers also use it in the study of heterocyclic chemistry to explore new reaction pathways and develop novel compounds with potential industrial or medicinal value.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,049.00
inventory 250mg
10-20 days ฿8,109.00
inventory 5g
10-20 days ฿55,575.00
inventory 1g
10-20 days ฿20,286.00
3-Bromo-6-nitroquinoline
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of more complex quinoline derivatives. Its bromo and nitro functional groups make it a versatile building block for various chemical reactions, including nucleophilic substitution and reduction processes. It is often employed in the development of pharmaceutical compounds, particularly those targeting infectious diseases, due to the biological activity associated with quinoline structures. Additionally, it finds application in the synthesis of dyes and pigments, where its nitro group contributes to color formation. Researchers also use it in the study of heterocyclic chemistry to explore new reaction pathways and develop novel compounds with potential industrial or medicinal value.
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