5-Bromo-8-nitroquinoline

≥95%

Reagent Code: #49058
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CAS Number 176967-80-9

science Other reagents with same CAS 176967-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.05 g/mol
Formula C₉H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD00466078
thermostat Physical Properties
Boiling Point 370.5°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 versatile intermediate for the preparation of more complex quinoline derivatives. Its bromo and nitro functional groups make it a valuable substrate for various chemical reactions, including nucleophilic substitution and catalytic cross-coupling processes. In medicinal chemistry, it is often explored for the development of potential pharmaceutical agents, particularly in the synthesis of compounds with antimicrobial or anticancer properties. Additionally, it is used in research settings to study the reactivity and transformation of quinoline-based structures, contributing to advancements in heterocyclic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,545.00
inventory 1g
10-20 days ฿18,288.00
inventory 250mg
10-20 days ฿7,236.00
inventory 5g
10-20 days ฿55,665.00

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5-Bromo-8-nitroquinoline
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This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex quinoline derivatives. Its bromo and nitro functional groups make it a valuable substrate for various chemical reactions, including nucleophilic substitution and catalytic cross-coupling processes. In medicinal chemistry, it is often explored for the development of potential pharmaceutical agents, particularly in the synthesis of compounds with antimicrobi

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the preparation of more complex quinoline derivatives. Its bromo and nitro functional groups make it a valuable substrate for various chemical reactions, including nucleophilic substitution and catalytic cross-coupling processes. In medicinal chemistry, it is often explored for the development of potential pharmaceutical agents, particularly in the synthesis of compounds with antimicrobial or anticancer properties. Additionally, it is used in research settings to study the reactivity and transformation of quinoline-based structures, contributing to advancements in heterocyclic chemistry.

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