7-Bromoquinolin-5-ol

95%

Reagent Code: #85584
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CAS Number 1261677-80-8

science Other reagents with same CAS 1261677-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.05 g/mol
Formula C₉H₆BrNO
badge Registry Numbers
MDL Number MFCD11878500
thermostat Physical Properties
Boiling Point 363.2±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activities, such as antimicrobial, anticancer, and anti-inflammatory agents. Its quinoline structure makes it valuable in the design of drugs targeting specific enzymes or receptors. Additionally, it is utilized in research for studying reaction mechanisms and developing novel chemical transformations.

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inventory 1g
10-20 days ฿35,073.00

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7-Bromoquinolin-5-ol
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Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activities, such as antimicrobial, anticancer, and anti-inflammatory agents. Its quinoline structure makes it valuable in the design of drugs targeting specific enzymes or receptors. Additionally, it is utilized in research for studying reaction mechanisms and developing nove

Used in organic synthesis as a building block for more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activities, such as antimicrobial, anticancer, and anti-inflammatory agents. Its quinoline structure makes it valuable in the design of drugs targeting specific enzymes or receptors. Additionally, it is utilized in research for studying reaction mechanisms and developing novel chemical transformations.

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