7-Bromoquinoline-4-carboxylic acid

≥95%

Reagent Code: #120892
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CAS Number 31009-04-8

science Other reagents with same CAS 31009-04-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.06 g/mol
Formula C₁₀H₆BrNO₂
badge Registry Numbers
MDL Number MFCD11108751
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

7-Bromoquinoline-4-carboxylic acid is primarily used in organic synthesis as a building block for the development of more complex chemical compounds. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of antimalarial and anticancer agents. Its quinoline core structure is valuable in medicinal chemistry for designing drugs that target specific biological pathways. Additionally, this compound is utilized in research to study its potential antimicrobial and anti-inflammatory properties. Its bromine substituent makes it a versatile reagent for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for various applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,535.00
inventory 100mg
10-20 days ฿2,772.00

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7-Bromoquinoline-4-carboxylic acid
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7-Bromoquinoline-4-carboxylic acid is primarily used in organic synthesis as a building block for the development of more complex chemical compounds. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of antimalarial and anticancer agents. Its quinoline core structure is valuable in medicinal chemistry for designing drugs that target specific biological pathways. Additionally, this compound is utilized in research to study its potential antimicrobial and a

7-Bromoquinoline-4-carboxylic acid is primarily used in organic synthesis as a building block for the development of more complex chemical compounds. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of antimalarial and anticancer agents. Its quinoline core structure is valuable in medicinal chemistry for designing drugs that target specific biological pathways. Additionally, this compound is utilized in research to study its potential antimicrobial and anti-inflammatory properties. Its bromine substituent makes it a versatile reagent for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for various applications.

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